Spaces:
Sleeping
Sleeping
<PubmedArticleSet> | |
<PubmedArticle> | |
<MedlineCitation Status="MEDLINE" Owner="NLM" IndexingMethod="Automated"> | |
<PMID Version="1">36473651</PMID> | |
<DateCompleted> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>15</Day> | |
</DateCompleted> | |
<DateRevised> | |
<Year>2024</Year> | |
<Month>06</Month> | |
<Day>05</Day> | |
</DateRevised> | |
<Article PubModel="Electronic"> | |
<Journal> | |
<ISSN IssnType="Electronic">1469-493X</ISSN> | |
<JournalIssue CitedMedium="Internet"> | |
<Volume>12</Volume> | |
<Issue>12</Issue> | |
<PubDate> | |
<Year>2022</Year> | |
<Month>Dec</Month> | |
<Day>07</Day> | |
</PubDate> | |
</JournalIssue> | |
<Title>The Cochrane database of systematic reviews</Title> | |
<ISOAbbreviation>Cochrane Database Syst Rev</ISOAbbreviation> | |
</Journal> | |
<ArticleTitle>Efficacy and safety of COVID-19 vaccines.</ArticleTitle> | |
<Pagination> | |
<StartPage>CD015477</StartPage> | |
<MedlinePgn>CD015477</MedlinePgn> | |
</Pagination> | |
<ELocationID EIdType="pii" ValidYN="Y">CD015477</ELocationID> | |
<ELocationID EIdType="doi" ValidYN="Y">10.1002/14651858.CD015477</ELocationID> | |
<Abstract> | |
<AbstractText Label="BACKGROUND">Different forms of vaccines have been developed | |
to prevent the SARS-CoV-2 virus and subsequent COVID-19 disease. Several are | |
in widespread use globally.  OBJECTIVES: To assess the efficacy and | |
safety of COVID-19 vaccines (as a full primary vaccination series or a | |
booster dose) against SARS-CoV-2.</AbstractText> | |
<AbstractText Label="SEARCH METHODS">We searched the Cochrane COVID-19 Study | |
Register and the COVID-19 L·OVE platform (last search date 5 November | |
2021). We also searched the WHO International Clinical Trials Registry | |
Platform, regulatory agency websites, and Retraction Watch.</AbstractText> | |
<AbstractText Label="SELECTION CRITERIA">We included randomized controlled | |
trials (RCTs) comparing COVID-19 vaccines to placebo, no vaccine, other | |
active vaccines, or other vaccine schedules.</AbstractText> | |
<AbstractText Label="DATA COLLECTION AND ANALYSIS">We used standard Cochrane | |
methods. We used GRADE to assess the certainty of evidence for all except | |
immunogenicity outcomes.  We synthesized data for each vaccine | |
separately and presented summary effect estimates with 95% confidence | |
intervals (CIs).  MAIN RESULTS: We included and analyzed 41 RCTs | |
assessing 12 different vaccines, including homologous and heterologous | |
vaccine schedules and the effect of booster doses. Thirty-two RCTs were | |
multicentre and five were multinational. The sample sizes of RCTs were 60 to | |
44,325 participants. Participants were aged: 18 years or older in 36 RCTs; | |
12 years or older in one RCT; 12 to 17 years in two RCTs; and three to 17 | |
years in two RCTs. Twenty-nine RCTs provided results for individuals aged | |
over 60 years, and three RCTs included immunocompromized patients. No trials | |
included pregnant women. Sixteen RCTs had two-month follow-up or less, 20 | |
RCTs had two to six months, and five RCTs had greater than six to 12 months | |
or less. Eighteen reports were based on preplanned interim analyses. Overall | |
risk of bias was low for all outcomes in eight RCTs, while 33 had concerns | |
for at least one outcome. We identified 343 registered RCTs with results not | |
yet available.  This abstract reports results for the critical outcomes | |
of confirmed symptomatic COVID-19, severe and critical COVID-19, and serious | |
adverse events only for the 10 WHO-approved vaccines. For remaining outcomes | |
and vaccines, see main text. The evidence for mortality was generally sparse | |
and of low or very low certainty for all WHO-approved vaccines, except | |
AD26.COV2.S (Janssen), which probably reduces the risk of all-cause | |
mortality (risk ratio (RR) 0.25, 95% CI 0.09 to 0.67; 1 RCT, 43,783 | |
participants; high-certainty evidence). Confirmed symptomatic COVID-19 | |
High-certainty evidence found that BNT162b2 (BioNtech/Fosun Pharma/Pfizer), | |
mRNA-1273 (ModernaTx), ChAdOx1 (Oxford/AstraZeneca), Ad26.COV2.S, BBIBP-CorV | |
(Sinopharm-Beijing), and BBV152 (Bharat Biotect) reduce the incidence of | |
symptomatic COVID-19 compared to placebo (vaccine efficacy (VE): BNT162b2: | |
97.84%, 95% CI 44.25% to 99.92%; 2 RCTs, 44,077 participants; mRNA-1273: | |
93.20%, 95% CI 91.06% to 94.83%; 2 RCTs, 31,632 participants; ChAdOx1: | |
70.23%, 95% CI 62.10% to 76.62%; 2 RCTs, 43,390 participants; Ad26.COV2.S: | |
66.90%, 95% CI 59.10% to 73.40%; 1 RCT, 39,058 participants; BBIBP-CorV: | |
78.10%, 95% CI 64.80% to 86.30%; 1 RCT, 25,463 participants; BBV152: 77.80%, | |
95% CI 65.20% to 86.40%; 1 RCT, 16,973 participants). Moderate-certainty | |
evidence found that NVX-CoV2373 (Novavax) probably reduces the incidence of | |
symptomatic COVID-19 compared to placebo (VE 82.91%, 95% CI 50.49% to | |
94.10%; 3 RCTs, 42,175 participants). There is low-certainty evidence for | |
CoronaVac (Sinovac) for this outcome (VE 69.81%, 95% CI 12.27% to 89.61%; 2 | |
RCTs, 19,852 participants). Severe or critical COVID-19 High-certainty | |
evidence found that BNT162b2, mRNA-1273, Ad26.COV2.S, and BBV152 result in a | |
large reduction in incidence of severe or critical disease due to COVID-19 | |
compared to placebo (VE: BNT162b2: 95.70%, 95% CI 73.90% to 99.90%; 1 RCT, | |
46,077 participants; mRNA-1273: 98.20%, 95% CI 92.80% to 99.60%; 1 RCT, | |
28,451 participants; AD26.COV2.S: 76.30%, 95% CI 57.90% to 87.50%; 1 RCT, | |
39,058 participants; BBV152: 93.40%, 95% CI 57.10% to 99.80%; 1 RCT, 16,976 | |
participants). Moderate-certainty evidence found that NVX-CoV2373 probably | |
reduces the incidence of severe or critical COVID-19 (VE 100.00%, 95% CI | |
86.99% to 100.00%; 1 RCT, 25,452 participants). Two trials reported high | |
efficacy of CoronaVac for severe or critical disease with wide CIs, but | |
these results could not be pooled. Serious adverse events (SAEs) mRNA-1273, | |
ChAdOx1 (Oxford-AstraZeneca)/SII-ChAdOx1 (Serum Institute of India), | |
Ad26.COV2.S, and BBV152 probably result in little or no difference in SAEs | |
compared to placebo (RR: mRNA-1273: 0.92, 95% CI 0.78 to 1.08; 2 RCTs, | |
34,072 participants; ChAdOx1/SII-ChAdOx1: 0.88, 95% CI 0.72 to 1.07; 7 RCTs, | |
58,182 participants; Ad26.COV2.S: 0.92, 95% CI 0.69 to 1.22; 1 RCT, 43,783 | |
participants); BBV152: 0.65, 95% CI 0.43 to 0.97; 1 RCT, 25,928 | |
participants). In each of these, the likely absolute difference in effects | |
was fewer than 5/1000 participants. Evidence for SAEs is uncertain for | |
BNT162b2, CoronaVac, BBIBP-CorV, and NVX-CoV2373 compared to placebo (RR: | |
BNT162b2: 1.30, 95% CI 0.55 to 3.07; 2 RCTs, 46,107 participants; CoronaVac: | |
0.97, 95% CI 0.62 to 1.51; 4 RCTs, 23,139 participants; BBIBP-CorV: 0.76, | |
95% CI 0.54 to 1.06; 1 RCT, 26,924 participants; NVX-CoV2373: 0.92, 95% CI | |
0.74 to 1.14; 4 RCTs, 38,802 participants). For the evaluation of | |
heterologous schedules, booster doses, and efficacy against variants of | |
concern, see main text of review.</AbstractText> | |
<AbstractText Label="AUTHORS' CONCLUSIONS">Compared to placebo, most vaccines | |
reduce, or likely reduce, the proportion of participants with confirmed | |
symptomatic COVID-19, and for some, there is high-certainty evidence that | |
they reduce severe or critical disease. There is probably little or no | |
difference between most vaccines and placebo for serious adverse events. | |
Over 300 registered RCTs are evaluating the efficacy of COVID-19 vaccines, | |
and this review is updated regularly on the COVID-NMA platform | |
(covid-nma.com). Implications for practice Due to the trial exclusions, | |
these results cannot be generalized to pregnant women, individuals with a | |
history of SARS-CoV-2 infection, or immunocompromized people. Most trials | |
had a short follow-up and were conducted before the emergence of variants of | |
concern. Implications for research Future research should evaluate the | |
long-term effect of vaccines, compare different vaccines and vaccine | |
schedules, assess vaccine efficacy and safety in specific populations, and | |
include outcomes such as preventing long COVID-19. Ongoing evaluation of | |
vaccine efficacy and effectiveness against emerging variants of concern is | |
also vital.</AbstractText> | |
<CopyrightInformation>Copyright © 2022 The Authors. Cochrane Database of | |
Systematic Reviews published by John Wiley & Sons, Ltd. on behalf of The | |
Cochrane Collaboration.</CopyrightInformation> | |
</Abstract> | |
<AuthorList CompleteYN="Y"> | |
<Author ValidYN="Y"> | |
<LastName>Graña</LastName> | |
<ForeName>Carolina</ForeName> | |
<Initials>C</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Ghosn</LastName> | |
<ForeName>Lina</ForeName> | |
<Initials>L</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Evrenoglou</LastName> | |
<ForeName>Theodoros</ForeName> | |
<Initials>T</Initials> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Jarde</LastName> | |
<ForeName>Alexander</ForeName> | |
<Initials>A</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Minozzi</LastName> | |
<ForeName>Silvia</ForeName> | |
<Initials>S</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Review Group on Drugs and Alcohol, Rome, Italy.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Bergman</LastName> | |
<ForeName>Hanna</ForeName> | |
<Initials>H</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Response, Cochrane, London, UK.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Buckley</LastName> | |
<ForeName>Brian S</ForeName> | |
<Initials>BS</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Response, Cochrane, London, UK.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Probyn</LastName> | |
<ForeName>Katrin</ForeName> | |
<Initials>K</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Response, Cochrane, London, UK.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Villanueva</LastName> | |
<ForeName>Gemma</ForeName> | |
<Initials>G</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Response, Cochrane, London, UK.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Henschke</LastName> | |
<ForeName>Nicholas</ForeName> | |
<Initials>N</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Response, Cochrane, London, UK.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Bonnet</LastName> | |
<ForeName>Hillary</ForeName> | |
<Initials>H</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Assi</LastName> | |
<ForeName>Rouba</ForeName> | |
<Initials>R</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Menon</LastName> | |
<ForeName>Sonia</ForeName> | |
<Initials>S</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Marti</LastName> | |
<ForeName>Melanie</ForeName> | |
<Initials>M</Initials> | |
<AffiliationInfo> | |
<Affiliation>Department of Immunization, Vaccines and Biologicals, World | |
Health Organization, Geneva, Switzerland.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Devane</LastName> | |
<ForeName>Declan</ForeName> | |
<Initials>D</Initials> | |
<AffiliationInfo> | |
<Affiliation>Evidence Synthesis Ireland, Cochrane Ireland and HRB-Trials | |
Methodology Research Network, National University of Ireland, | |
Galway, Ireland.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Mallon</LastName> | |
<ForeName>Patrick</ForeName> | |
<Initials>P</Initials> | |
<AffiliationInfo> | |
<Affiliation>UCD Centre for Experimental Pathogen Host Research and UCD | |
School of Medicine, University College Dublin, Dublin, Ireland.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Lelievre</LastName> | |
<ForeName>Jean-Daniel</ForeName> | |
<Initials>JD</Initials> | |
<AffiliationInfo> | |
<Affiliation>Department of Clinical Immunology and Infectious Diseases, | |
Henri Mondor Hospital, Vaccine Research Institute, Université | |
Paris Est Créteil, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Askie</LastName> | |
<ForeName>Lisa M</ForeName> | |
<Initials>LM</Initials> | |
<AffiliationInfo> | |
<Affiliation>Quality Assurance Norms and Standards Department, World | |
Health Organization, Geneva, Switzerland.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Kredo</LastName> | |
<ForeName>Tamara</ForeName> | |
<Initials>T</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane South Africa, South African Medical Research | |
Council, Cape Town, South Africa.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Ferrand</LastName> | |
<ForeName>Gabriel</ForeName> | |
<Initials>G</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Davidson</LastName> | |
<ForeName>Mauricia</ForeName> | |
<Initials>M</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Riveros</LastName> | |
<ForeName>Carolina</ForeName> | |
<Initials>C</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Tovey</LastName> | |
<ForeName>David</ForeName> | |
<Initials>D</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Meerpohl</LastName> | |
<ForeName>Joerg J</ForeName> | |
<Initials>JJ</Initials> | |
<AffiliationInfo> | |
<Affiliation>Institute for Evidence in Medicine, Medical Center & | |
Faculty of Medicine, University of Freiburg, Freiburg, Germany.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Cochrane Germany, Cochrane Germany Foundation, Freiburg, | |
Germany.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Grasselli</LastName> | |
<ForeName>Giacomo</ForeName> | |
<Initials>G</Initials> | |
<AffiliationInfo> | |
<Affiliation>Department of Anesthesia, Intensive Care and Emergency, | |
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, | |
Department of Pathophysiology and Transplantation, University of | |
Milan, Milan, Italy.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Rada</LastName> | |
<ForeName>Gabriel</ForeName> | |
<Initials>G</Initials> | |
<AffiliationInfo> | |
<Affiliation>Epistemonikos Foundation, Santiago, Chile.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>UC Evidence Center, Cochrane Chile Associated Center, | |
Pontificia Universidad Católica de Chile, Santiago, Chile.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Hróbjartsson</LastName> | |
<ForeName>Asbjørn</ForeName> | |
<Initials>A</Initials> | |
<AffiliationInfo> | |
<Affiliation>Centre for Evidence Based Medicine Odense (CEBMO) and | |
Cochrane Denmark, University of Southern Denmark, Odense, Denmark.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Open Patient data Explorative Network (OPEN), Odense | |
University Hospital, Odense, Denmark.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Ravaud</LastName> | |
<ForeName>Philippe</ForeName> | |
<Initials>P</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Chaimani</LastName> | |
<ForeName>Anna</ForeName> | |
<Initials>A</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
<Author ValidYN="Y"> | |
<LastName>Boutron</LastName> | |
<ForeName>Isabelle</ForeName> | |
<Initials>I</Initials> | |
<AffiliationInfo> | |
<Affiliation>Cochrane France, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
<AffiliationInfo> | |
<Affiliation>Centre of Research in Epidemiology and Statistics (CRESS), | |
INSERM, INRAE, Université de Paris, Paris, France.</Affiliation> | |
</AffiliationInfo> | |
</Author> | |
</AuthorList> | |
<Language>eng</Language> | |
<GrantList CompleteYN="Y"> | |
<Grant> | |
<GrantID>001</GrantID> | |
<Acronym>WHO_</Acronym> | |
<Agency>World Health Organization</Agency> | |
<Country>International</Country> | |
</Grant> | |
</GrantList> | |
<PublicationTypeList> | |
<PublicationType UI="D016428">Journal Article</PublicationType> | |
<PublicationType UI="D016454">Review</PublicationType> | |
<PublicationType UI="D000078182">Systematic Review</PublicationType> | |
</PublicationTypeList> | |
<ArticleDate DateType="Electronic"> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>07</Day> | |
</ArticleDate> | |
</Article> | |
<MedlineJournalInfo> | |
<Country>England</Country> | |
<MedlineTA>Cochrane Database Syst Rev</MedlineTA> | |
<NlmUniqueID>100909747</NlmUniqueID> | |
<ISSNLinking>1361-6137</ISSNLinking> | |
</MedlineJournalInfo> | |
<ChemicalList> | |
<Chemical> | |
<RegistryNumber>0</RegistryNumber> | |
<NameOfSubstance UI="C000722216">sinovac COVID-19 vaccine</NameOfSubstance> | |
</Chemical> | |
<Chemical> | |
<RegistryNumber>0</RegistryNumber> | |
<NameOfSubstance UI="C000722768">BIBP COVID-19 vaccine</NameOfSubstance> | |
</Chemical> | |
<Chemical> | |
<RegistryNumber>76JZE5DSN6</RegistryNumber> | |
<NameOfSubstance UI="C000722386">BBV152 COVID-19 vaccine</NameOfSubstance> | |
</Chemical> | |
<Chemical> | |
<RegistryNumber>EPK39PL4R4</RegistryNumber> | |
<NameOfSubstance UI="D000090983">2019-nCoV Vaccine mRNA-1273</NameOfSubstance> | |
</Chemical> | |
</ChemicalList> | |
<CitationSubset>IM</CitationSubset> | |
<MeshHeadingList> | |
<MeshHeading> | |
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D000293" MajorTopicYN="N">Adolescent</DescriptorName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D000090983" MajorTopicYN="Y">2019-nCoV Vaccine mRNA-1273</DescriptorName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D000086382" MajorTopicYN="Y">COVID-19</DescriptorName> | |
<QualifierName UI="Q000517" MajorTopicYN="N">prevention & control</QualifierName> | |
</MeshHeading> | |
<MeshHeading> | |
<DescriptorName UI="D000086402" MajorTopicYN="N">SARS-CoV-2</DescriptorName> | |
</MeshHeading> | |
</MeshHeadingList> | |
<CoiStatement>Carolina Graña: none known. Lina Ghosn: none known. Theodoros | |
Evrenoglou: none known. Alexander Jarde: none known. Silvia Minozzi: no relevant | |
interests; Joint Co‐ordinating Editor and Method editor of the Drugs and | |
Alcohol Group. Hanna Bergman: Cochrane Response – consultant; WHO – | |
grant/contract (Cochrane Response was commissioned by the WHO to perform review | |
tasks that contribute to this publication). . Brian Buckley: none known. . | |
Katrin Probyn: Cochrane Response – consultant; WHO – consultant | |
(Cochrane Response was commissioned to perform review tasks that contribute to this | |
publication). . Gemma Villanueva: Cochrane Response – employment | |
(Cochrane Response has been commissioned by WHO to perform parts of this systematic | |
review). . Nicholas Henschke: Cochrane Response – consultant; WHO | |
– consultant (Cochrane Response was commissioned by the WHO to perform review | |
tasks that contributed to this publication). . Hillary Bonnet: none known. | |
Rouba Assi: none known. Sonia Menon: P95 – consultant. Melanie Marti: no | |
relevant interests; Medical Officer at WHO. Declan Devane: Health Research Board | |
(HRB) – grant/contract; registered nurse and registered midwife but no longer | |
in clinical practice; Editor, Cochrane Pregnancy and Childbirth Group. Patrick | |
Mallon: AstraZeneca – Advisory Board; spoken of vaccine effectiveness to | |
media (print, online, and live); works as a consultant in a hospital that provides | |
vaccinations; employed by St Vincent's University Hospital. Jean‐Daniel | |
Lelievre: no relevant interests; published numerous interviews in the national press | |
on the subject of COVID vaccination; Head of the Department of Infectious Diseases | |
and Clinical Immunology CHU Henri Mondor APHP, Créteil; WHO (IVRI‐AC): | |
expert Vaccelarate (European project on COVID19 Vaccine): head of WP; involved with | |
COVICOMPARE P et M Studies (APHP, INSERM) (public fundings). . Lisa Askie: no | |
relevant interests; Co‐convenor, Cochrane Prospective Meta‐analysis | |
Methods Group. Tamara Kredo: no relevant interests; Medical Officer in an Infectious | |
Diseases Clinic at Tygerberg Hospital, Stellenbosch University. Gabriel Ferrand: | |
none known. Mauricia Davidson: none known. Carolina Riveros: no relevant interests; | |
works as an epidemiologist. David Tovey: no relevant interests; Emeritus Editor in | |
Chief, Feedback Editors for 2 Cochrane review groups. Joerg J Meerpohl: no relevant | |
interests; member of the German Standing Vaccination Committee (STIKO). Giacomo | |
Grasselli: Pfizer – speaking engagement. Gabriel Rada: none known. | |
Asbjørn Hróbjartsson: no relevant interests; Cochrane Methodology Review | |
Group Editor. Philippe Ravaud: no relevant interests; involved with Mariette | |
CORIMUNO‐19 Collaborative 2021, the Ministry of Health, Programme Hospitalier | |
de Recherche Clinique, Foundation for Medical Research, and AP‐HP Foundation. | |
Anna Chaimani: none known. Isabelle Boutron: no relevant interests; member of | |
Cochrane Editorial Board.</CoiStatement> | |
</MedlineCitation> | |
<PubmedData> | |
<History> | |
<PubMedPubDate PubStatus="entrez"> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>6</Day> | |
<Hour>19</Hour> | |
<Minute>26</Minute> | |
</PubMedPubDate> | |
<PubMedPubDate PubStatus="pubmed"> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>7</Day> | |
<Hour>6</Hour> | |
<Minute>0</Minute> | |
</PubMedPubDate> | |
<PubMedPubDate PubStatus="medline"> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>15</Day> | |
<Hour>6</Hour> | |
<Minute>0</Minute> | |
</PubMedPubDate> | |
<PubMedPubDate PubStatus="pmc-release"> | |
<Year>2022</Year> | |
<Month>12</Month> | |
<Day>7</Day> | |
</PubMedPubDate> | |
</History> | |
<PublicationStatus>epublish</PublicationStatus> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">36473651</ArticleId> | |
<ArticleId IdType="pmc">PMC9726273</ArticleId> | |
<ArticleId IdType="doi">10.1002/14651858.CD015477</ArticleId> | |
</ArticleIdList> | |
<ReferenceList> | |
<Title>References to studies included in this review</Title> | |
<ReferenceList> | |
<Title>Ali 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Ali K, Berman G, Zhou H, Deng W, Faughnan V, Coronado-Voges M, et | |
al. Evaluation of mRNA-1273 SARS-CoV-2 vaccine in adolescents. New | |
England Journal of Medicine 2021;385(24):2241-51.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8385554</ArticleId> | |
<ArticleId IdType="pubmed">34379915</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Al Kaabi 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Al Kaabi N, Zhang Y, Xia S, Yang Y, Al Qahtani MM, Abdulrazzaq N, | |
et al. Effect of 2 inactivated SARS-CoV-2 vaccines on symptomatic | |
COVID-19 infection in adults: a randomized clinical trial. JAMA | |
2021;326(1):35-45.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8156175</ArticleId> | |
<ArticleId IdType="pubmed">34037666</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Asano 2022 {published data only}</Title> | |
<Reference> | |
<Citation>Asano M, Okada H, Itoh Y, Hirata H, Ishikawa K, Yoshida E, et al. | |
Immunogenicity and safety of AZD1222 (ChAdOx1 nCoV-19) against | |
SARS-CoV-2 in Japan: a double-blind, randomized controlled phase 1/2 | |
trial. International Journal of Infectious Diseases 2022;114:165-74.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8531242</ArticleId> | |
<ArticleId IdType="pubmed">34688944</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Bonelli 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Bonelli M, Mrak D, Tobudic S, Sieghart D, Koblischke M, Mandl P, | |
et al. Additional heterologous versus homologous booster vaccination in | |
immunosuppressed patients without SARS-CoV-2 antibody seroconversion | |
after primary mRNA vaccination: a randomized controlled trial. medRxiv | |
2021 [Preprint]. [DOI: 10.1101/2021.09.05.21263125]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.05.21263125</ArticleId> | |
<ArticleId IdType="pubmed">35027397</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Bueno 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Bueno SM, Abarca K, González PA, Gálvez NM, Soto JA, | |
Duarte LF, et al. Interim report: safety and immunogenicity of an | |
inactivated vaccine against SARS-CoV-2 in healthy Chilean adults in a | |
phase 3 clinical trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.03.31.21254494]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.03.31.21254494</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Bueno SM, Abarca K, González PA, Gálvez NM, Soto JA, | |
Duarte LF, et al. Safety and immunogenicity of an inactivated SARS-CoV-2 | |
vaccine in a subgroup of healthy adults in Chile. Clinical Infectious | |
Diseases 2021 Sep 19 [Epub ahead of print]. [DOI: 10.1093/cid/ciab823]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1093/cid/ciab823</ArticleId> | |
<ArticleId IdType="pmc">PMC9402626</ArticleId> | |
<ArticleId IdType="pubmed">34537835</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Clemens 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Clemens SA, Folegatti PM, Emary KR, Weckx LY, Ratcliff J, Bibi S, | |
et al. Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 | |
lineages circulating in Brazil. Nature Communications 2021;12(1):5861.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8494913</ArticleId> | |
<ArticleId IdType="pubmed">34615860</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Dunkle 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Dunkle LM, Kotloff KL, Gay CL, Áñez G, Adelglass JM, | |
Barrat Hernández AQ, et al. Efficacy and safety of NVX-CoV2373 in | |
adults in the United States and Mexico. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.10.05.21264567]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.10.05.21264567</ArticleId> | |
<ArticleId IdType="pmc">PMC8693692</ArticleId> | |
<ArticleId IdType="pubmed">34910859</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ella 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Ella R, Vadrevu KM, Jogdand H, Prasad S, Reddy S, Sarangi V, et | |
al. A Phase 1: safety and immunogenicity trial of an inactivated | |
SARS-CoV-2 vaccine-BBV152. medRxiv 2020 [Preprint]. [DOI: | |
10.1101/2020.12.11.20210419]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2020.12.11.20210419</ArticleId> | |
<ArticleId IdType="pmc">PMC7825810</ArticleId> | |
<ArticleId IdType="pubmed">33485468</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Ella R, Vadrevu KM, Jogdand H, Prasad S, Reddy S, Sarangi V, et | |
al. Safety and immunogenicity of an inactivated SARS-CoV-2 vaccine, | |
BBV152: a double-blind, randomized, phase 1 trial. Lancet Infectious | |
Diseases 2021;21(5):637-46.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7825810</ArticleId> | |
<ArticleId IdType="pubmed">33485468</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ella 2021b {published data only}</Title> | |
<Reference> | |
<Citation>Ella R, Reddy S, Blackwelder W, Potdar V, Yadav P, Sarangi V, et | |
al. Efficacy, safety, and lot to lot immunogenicity of an inactivated | |
SARS-CoV-2 vaccine (BBV152): a double-blind, randomized, controlled | |
phase 3 trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.06.30.21259439]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.06.30.21259439</ArticleId> | |
<ArticleId IdType="pmc">PMC8584828</ArticleId> | |
<ArticleId IdType="pubmed">34774196</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>El Sahly 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et | |
al. Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. New England | |
Journal of Medicine 2021;384(5):403-16.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7787219</ArticleId> | |
<ArticleId IdType="pubmed">33378609</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>El Sahly HM, Baden LR, Essink B, Doblecki-Lewis S, Martin JM, | |
Anderson EJ, et al. Efficacy of the mRNA-1273 SARS-CoV-2 vaccine at | |
completion of blinded phase. New England Journal of Medicine | |
2021;385(19):1774-85.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8482810</ArticleId> | |
<ArticleId IdType="pubmed">34551225</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Food and Drug Administration. Vaccines and Related Biological | |
Products Advisory Committee Meeting; December 17, 2020; FDA Briefing | |
Document: Moderna COVID-19 vaccine. www.fda.gov/media/144434/download | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Emary 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Emary KR, Golubchik T, Aley PK, Ariani CV, Angus B, Bibi S, et al. | |
Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant | |
of concern 202012/01 (B.1.1.7): an exploratory analysis of a randomized | |
controlled trial. Lancet 2021;397(10282):1351-62.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8009612</ArticleId> | |
<ArticleId IdType="pubmed">33798499</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Fadlyana 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Fadlyana E, Rusmil K, Tarigan R, Rahmadi AR, Prodjosoewojo S, | |
Sofiatin Y, et al. A phase III, observer-blind, randomized, | |
placebo-controlled study of the efficacy, safety, and immunogenicity of | |
SARS-CoV-2 inactivated vaccine in healthy adults aged | |
18–59 years: an interim analysis in Indonesia. Vaccine | |
2021;39(44):6520-8.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8461222</ArticleId> | |
<ArticleId IdType="pubmed">34620531</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Falsey 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Falsey AR, Sobieszczyk ME, Hirsch I, Sproule S, Robb ML, Corey L, | |
et al. Phase 3 safety and efficacy of AZD1222 (ChAdOx1 nCoV-19) Covid-19 | |
vaccine. New England Journal of Medicine 2021;385(25):2348-60.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8522798</ArticleId> | |
<ArticleId IdType="pubmed">34587382</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Formica 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Formica N, Mallory R, Albert G, Robinson M, Plested JS, Cho I, et | |
al. Different dose regimens of a SARS-CoV-2 recombinant spike protein | |
vaccine (NVX-CoV2373) in younger and older adults: a phase 2 randomized | |
placebo-controlled trial. PLOS Medicine 2021;18(10):e1003769.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8486115</ArticleId> | |
<ArticleId IdType="pubmed">34597298</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Formica N, Mallory R, Albert G, Robinson M, Plested JS, Cho I, et | |
al. Evaluation of a SARS-CoV-2 vaccine NVX-CoV2373 in younger and older | |
adults. medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.02.26.21252482]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.02.26.21252482</ArticleId> | |
<ArticleId IdType="pmc">PMC8486115</ArticleId> | |
<ArticleId IdType="pubmed">34597298</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Frenck 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Frenck RW Jr, Klein NP, Kitchin N, Gurtman A, Absalon J, Lockhart | |
S, et al. Safety, immunogenicity, and efficacy of the BNT162b2 Covid-19 | |
vaccine in adolescents. New England Journal of Medicine | |
2021;385(3):239-50.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8174030</ArticleId> | |
<ArticleId IdType="pubmed">34043894</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Guo 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Guo W, Duan K, Zhang Y, Yuan Z, Zhang YB, Wang Z, et al. Safety | |
and immunogenicity of an inactivated SARS-CoV-2 vaccine in healthy | |
adults aged 18 years or older: a randomized, double-blind, | |
placebo-controlled, phase 1/2 trial. eClinicalMedicine 2021;38:101010.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8260504</ArticleId> | |
<ArticleId IdType="pubmed">34250456</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Hall 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Hall VG, Ferreira VH, Ku T, Ierullo M, Majchrzak-Kita B, Chaparro | |
C, et al. Randomized trial of a third dose of mRNA-1273 vaccine in | |
transplant recipients. New England Journal of Medicine | |
2021;385(13):1244-6.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8385563</ArticleId> | |
<ArticleId IdType="pubmed">34379917</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Han 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Han B, Song Y, Li C, Yang W, Ma Q, Jiang Z, et al. Safety, | |
tolerability, and immunogenicity of an inactivated SARS-CoV-2 vaccine | |
(CoronaVac) in healthy children and adolescents: a double-blind, | |
randomized, controlled, phase 1/2 clinical trial. Lancet Infectious | |
Diseases 2021;21(12):1645-53.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8238449</ArticleId> | |
<ArticleId IdType="pubmed">34197764</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Heath 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et | |
al. Safety and efficacy of NVX-CoV2373 Covid-19 vaccine. New England | |
Journal of Medicine 2021;385(13):1172-83.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8262625</ArticleId> | |
<ArticleId IdType="pubmed">34192426</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et | |
al . Efficacy of the NVX-CoV2373 Covid-19 vaccine against the B. | |
1.1.7 variant. medRxiv 2021 [Preprint].</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Keech 2020 {published data only}</Title> | |
<Reference> | |
<Citation>Keech C, Albert G, Cho I, Robertson A, Reed P, Neal S, et al. | |
Phase 1-2 trial of a SARS-CoV-2 recombinant spike protein nanoparticle | |
vaccine. New England Journal of Medicine  2020;383:2320-32.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7494251</ArticleId> | |
<ArticleId IdType="pubmed">32877576</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Kremsner 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Kremsner PG, Ahuad Guerrero RA, Arana-Arri E, Aroca Martinez GJ, | |
Bonten M, Chandler R, et al. Efficacy and safety of the CVnCoV | |
SARS-CoV-2 mRNA vaccine candidate: results from Herald, a phase 2b/3, | |
randomized, observer-blinded, placebo-controlled clinical trial in ten | |
countries in Europe and Latin America. SSRN 2021 [Preprint]. [DOI: | |
10.2139/ssrn.3911826]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.2139/ssrn.3911826</ArticleId> | |
<ArticleId IdType="pmc">PMC8610426</ArticleId> | |
<ArticleId IdType="pubmed">34826381</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Kulkarni 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Kulkarni PS, Padmapriyadarsini C, Vekemans J, Bavdekar A, Gupta M, | |
Kulkarni P, et al. A phase 2/3, observer-blind, randomized, controlled | |
study to assess the safety and immunogenicity of SII-ChAdOx1 nCOV-19 | |
(COVID-19 vaccine) in adults in India. eClinicalMedicine 2021;42:101218.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8629682</ArticleId> | |
<ArticleId IdType="pubmed">34870133</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Li 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Li J, Hou L, Guo X, Jin P, Wu S, Zhu J, et al. Heterologous | |
prime-boost immunization with CoronaVac and Convidecia. medRxiv 2021 | |
[Preprint]. [DOI: 10.1101/2021.09.03.21263062]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.03.21263062</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Liu 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Liu X, Shaw RH, Stuart AS, Greenland M, Aley PK, Andrews NJ, et | |
al. Safety and immunogenicity of heterologous versus homologous | |
prime-boost schedules with an adenoviral vectored and mRNA COVID-19 | |
vaccine (Com-COV): a single-blind, randomized, non-inferiority trial. | |
Lancet 2021;398(10303):856-69.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8346248</ArticleId> | |
<ArticleId IdType="pubmed">34370971</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Liu X, Shaw RH, Stuart AS, Greenland M, Aley PK, Andrews NJ, et | |
al. Safety and immunogenicity report from the Com-COV Study – a | |
single-blind randomized non-inferiority trial comparing heterologous and | |
homologous prime-boost schedules with an adenoviral vectored and mRNA | |
COVID-19 vaccine. SSRN 2021 [Preprint]. [DOI: 10.2139/ssrn.3874014]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.2139/ssrn.3874014</ArticleId> | |
<ArticleId IdType="pmc">PMC8346248</ArticleId> | |
<ArticleId IdType="pubmed">34370971</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Logunov 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Logunov DY, Dolzhikova IV, Shcheblyakov DV, Tukhvatulin AI, | |
Zubkova OV, Dzharullaeva AS, et al. Safety and efficacy of an rAd26 and | |
rAd5 vector-based heterologous prime-boost COVID-19 vaccine: an interim | |
analysis of a randomized controlled phase 3 trial in Russia. Lancet | |
2021;397(10275):671-81.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7852454</ArticleId> | |
<ArticleId IdType="pubmed">33545094</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Madhi 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Madhi SA, Koen AL, Izu A, Fairlie L, Cutland CL, Baillie V, et al. | |
Safety and immunogenicity of the ChAdOx1 nCoV-19 (AZD1222) vaccine | |
against SARS-CoV-2 in people living with and without HIV in South | |
Africa: an interim analysis of a randomized, double-blind, | |
placebo-controlled, phase 1B/2A trial. Lancet HIV 2021;8(9):e568-80.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8372504</ArticleId> | |
<ArticleId IdType="pubmed">34416193</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Madhi 2021b {published data only}</Title> | |
<Reference> | |
<Citation>Madhi SA, Baillie V, Cutland CL, Voysey M, Koen AL, Fairlie L, et | |
al. Efficacy of the ChAdOx1 nCoV-19 Covid-19 vaccine against the B.1.351 | |
variant. New England Journal of Medicine 2021;384(20):1885-98.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7993410</ArticleId> | |
<ArticleId IdType="pubmed">33725432</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Mok 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Mok C, Cheng S, Chen C, Yiu K, Chan TO, Lai KC, et al. A RCT of a | |
third dose CoronaVac or BNT162b2 vaccine in adults with two doses of | |
CoronaVac. medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.11.02.21265843]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.11.02.21265843</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Palacios 2020 {published data only}</Title> | |
<Reference> | |
<Citation>Palacios R, Patiño EG, Oliveira Piorelli R, Conde MT, Batista | |
AP, Zeng G, et al. Double-blind, randomized, placebo-controlled phase | |
III clinical trial to evaluate the efficacy and safety of treating | |
healthcare professionals with the adsorbed COVID-19 (inactivated) | |
vaccine manufactured by Sinovac – PROFISCOV: a structured summary | |
of a study protocol for a randomized controlled trial. Trials | |
2020;21(1):853.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7558252</ArticleId> | |
<ArticleId IdType="pubmed">33059771</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sablerolles 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Sablerolles RS, Rietdijk WJ, Goorhuis A, Postma DF, Visser LG, | |
Geers D, et al. Immunogenicity and reactogenicity of booster | |
vaccinations after Ad26.COV2.S priming. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.10.18.21264979]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.10.18.21264979</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sadoff 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. Vaccines and related biological | |
products Advisory Committee Meeting; February 26, 2021; FDA briefing | |
document: Janssen Ad26.COV2.S vaccine for the prevention of COVID-19. | |
www.fda.gov/media/146217/download (accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
<Reference> | |
<Citation>Sadoff J, Le Gars M, Shukarev G, Heerwegh D, Truyers C, Groot AM, | |
et al. Interim results of a Phase 1-2a trial of Ad26.COV2.S Covid-19 | |
vaccine. New England Journal of Medicine 2021;384(19):1824-35.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7821985</ArticleId> | |
<ArticleId IdType="pubmed">33440088</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Sadoff J, Le Gars M, Shukarev G, Heerwegh D, Truyers C, Groot AM, | |
et al. Safety and immunogenicity of the Ad26.COV2.S COVID-19 vaccine | |
candidate: interim results of a phase 1/2a, double-blind, randomized, | |
placebo-controlled trial. medRxiv 2020 [Preprint]. [DOI: | |
10.1101/2020.09.23.20199604]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2020.09.23.20199604</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sadoff 2021b {published data only}</Title> | |
<Reference> | |
<Citation>Sadoff J, Gray G, Vandebosch A, Cárdenas V, Shukarev G, | |
Grinsztejn B, et al. Safety and efficacy of single-dose Ad26.COV2.S | |
vaccine against Covid-19. New England Journal of Medicine | |
2021;384(23):2187-201.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8220996</ArticleId> | |
<ArticleId IdType="pubmed">33882225</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Shinde 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Shinde V, Bhikha S, Hoosain Z, Archary M, Bhorat Q, Fairlie L, et | |
al. Efficacy of NVX-CoV2373 Covid-19 vaccine against the B.1.351 | |
variant. New England Journal of Medicine 2021;384(20):1899-909.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8091623</ArticleId> | |
<ArticleId IdType="pubmed">33951374</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Shinde V, Bhikha S, Hoosain Z, Archary M, Bhorat Q, Fairlie L, et | |
al. Preliminary efficacy of the NVX-CoV2373 Covid-19 vaccine against the | |
B.1.351 variant. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.02.25.21252477]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.02.25.21252477</ArticleId> | |
<ArticleId IdType="pmc">PMC8091623</ArticleId> | |
<ArticleId IdType="pubmed">33951374</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Tanriover 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Tanriover MD, Doğanay HL, Akova M, Güner HR, Azap A, | |
Akhan S, et al. Efficacy and safety of an inactivated whole-virion | |
SARS-CoV-2 vaccine (CoronaVac): interim results of a double-blind, | |
randomized, placebo-controlled, phase 3 trial in Turkey. Lancet | |
2021;398(10296):213-22.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8266301</ArticleId> | |
<ArticleId IdType="pubmed">34246358</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Thomas 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. Vaccines and related biological | |
products Advisory Committee Meeting; December 10, 2020; FDA briefing | |
document: Pfizer-BioNTech COVID-19 vaccine. | |
www.fda.gov/media/144245/download (accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
<Reference> | |
<Citation>Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, | |
et al. Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. New | |
England Journal of Medicine 2020;383(27):2603-15.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7745181</ArticleId> | |
<ArticleId IdType="pubmed">33301246</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Thomas SJ, Moreira ED Jr, Kitchin N, Absalon J, Gurtman A, | |
Lockhart S, et al. Safety and efficacy of the BNT162b2 mRNA Covid-19 | |
vaccine through 6 months. New England Journal of Medicine | |
2021;385(19):1761-773.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8461570</ArticleId> | |
<ArticleId IdType="pubmed">34525277</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Thomas SJ, Moreira ED Jr, Kitchin N, Absalon J, Gurtman A, | |
Lockhart S, et al. Six month safety and efficacy of the BNT162b2 mRNA | |
COVID-19 vaccine. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.07.28.21261159]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.07.28.21261159</ArticleId> | |
<ArticleId IdType="pmc">PMC8461570</ArticleId> | |
<ArticleId IdType="pubmed">34525277</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Toledo‐Romani 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Toledo-Romani ME, Garcia-Carmenate M, Silva-Valenzuela C, | |
Baldoquin-Rodriguez W, Martínez-Pérez M, | |
Rodríguez-González M, et al. Safety and efficacy of the two | |
doses conjugated protein-based SOBERANA-02 COVID-19 vaccine and of a | |
heterologous three-dose combination with SOBERANA-PLUS: double-blind, | |
randomized, placebo-controlled phase 3 clinical trial. medRxiv 2021 | |
[Preprint]. [DOI: 10.1101/2021.10.31.21265703]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.10.31.21265703</ArticleId> | |
<ArticleId IdType="pmc">PMC9803910</ArticleId> | |
<ArticleId IdType="pubmed">36618081</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Voysey 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Folegatti PM, Ewer KJ, Aley PK, Angus B, Becker S, | |
Belij-Rammerstorfer S, et al. Safety and immunogenicity of the ChAdOx1 | |
nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, | |
single-blind, randomized controlled trial. Lancet | |
2020;396(10249):467-78. [PMID: ]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7445431</ArticleId> | |
<ArticleId IdType="pubmed">32702298</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Voysey M, Clemens SA, Madhi SA, Weckx LY, Folegatti PM, Aley PK, | |
et al. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) | |
against SARS-CoV-2: an interim analysis of four randomized controlled | |
trials in Brazil, South Africa, and the UK. Lancet | |
2021;397(10269):99-111. [PMID: ]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7723445</ArticleId> | |
<ArticleId IdType="pubmed">33306989</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Walsh 2020 {published data only}</Title> | |
<Reference> | |
<Citation>Walsh EE, Frenck R, Falsey AR, Kitchin N, Absalon J, Gurtman A, et | |
al. RNA-based COVID-19 vaccine BNT162b2 selected for a pivotal efficacy | |
study. medRxiv 2020 [Preprint]. [DOI: 10.1101/2020.08.17.20176651]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2020.08.17.20176651</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Walsh EE, Frenck RW Jr, Falsey AR, Kitchin N, Absalon J, Gurtman | |
A, et al. Safety and immunogenicity of two RNA-based Covid-19 vaccine | |
candidates. New England Journal of Medicine 2020;383(25):2439-50.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7583697</ArticleId> | |
<ArticleId IdType="pubmed">33053279</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Wu 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Wu Z, Hu Y, Xu M, Chen Z, Yang W, Jiang Z, et al. Safety, | |
tolerability, and immunogenicity of an inactivated SARS-CoV-2 vaccine | |
(CoronaVac) in healthy adults aged 60 years and older: a randomized, | |
double-blind, placebo-controlled, phase 1/2 clinical trial. Lancet | |
Infectious Diseases 2021;21(6):803-12.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7906628</ArticleId> | |
<ArticleId IdType="pubmed">33548194</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Xia 2020 {published data only}</Title> | |
<Reference> | |
<Citation>Xia S, Duan K, Zhang Y, Zhao D, Zhang H, Xie Z, et al. Effect of | |
an inactivated vaccine against SARS-CoV-2 on safety and immunogenicity | |
outcomes: interim analysis of 2 randomized clinical trials. JAMA | |
2020;324(10):951-60.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7426884</ArticleId> | |
<ArticleId IdType="pubmed">32789505</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
<Reference> | |
<Citation>Xia S, Zhang Y, Wang Y, Wang H, Yang Y, Gao GF, et al. Safety and | |
immunogenicity of an inactivated SARS-CoV-2 vaccine, BBIBP-CorV: a | |
randomized, double-blind, placebo-controlled, phase 1/2 trial. Lancet | |
Infectious Diseases 2020;21(1):39-51.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7561304</ArticleId> | |
<ArticleId IdType="pubmed">33069281</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Xia 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Xia S, Zhang Y, Wang Y, Wang H, Yang Y, Gao GF, et al. Safety and | |
immunogenicity of an inactivated COVID-19 vaccine, BBIBP-CorV, in people | |
younger than 18 years: a randomized, double-blind, controlled, phase 1/2 | |
trial. Lancet Infectious Diseases 2021;22(2):196-208.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8443232</ArticleId> | |
<ArticleId IdType="pubmed">34536349</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zhang 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Zhang Y, Zeng G, Pan H, Li C, Hu Y, Chu K, et al. Safety, | |
tolerability, and immunogenicity of an inactivated SARS-CoV-2 vaccine in | |
healthy adults aged 18–59 years: a randomized, double-blind, | |
placebo-controlled, phase 1/2 clinical trial. Lancet Infectious Diseases | |
2021;21(2):181-92.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7832443</ArticleId> | |
<ArticleId IdType="pubmed">33217362</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>References to studies excluded from this review</Title> | |
<ReferenceList> | |
<Title>Baden 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Baden LR, El Sahly HM, Essink B, Follmann D, Neuzil KM, August A, | |
et al. Covid-19 in the phase 3 trial of mRNA-1273 during the | |
Delta-variant surge. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.17.21263624]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.17.21263624</ArticleId> | |
<ArticleId IdType="pmc">PMC8609569</ArticleId> | |
<ArticleId IdType="pubmed">34731553</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Barrett 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Barrett JR, Belij-Rammerstorfer S, Dold C, Ewer KJ, Folegatti PM, | |
Gilbride C, et al. Phase 1/2 trial of SARS-CoV-2 vaccine ChAdOx1 nCoV-19 | |
with a booster dose induces multifunctional antibody responses. Nature | |
Medicine 2021;27(2):279-88.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33335322</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ewer 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Ewer KJ, Barrett JR, Belij-Rammerstorfer S, Sharpe H, Makinson R, | |
Morter R, et al. T cell and antibody responses induced by a single dose | |
of ChAdOx1 nCoV-19 (AZD1222) vaccine in a phase 1/2 clinical trial. | |
Nature Medicine 2021;27(2):270-8.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33335323</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Flaxman 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Flaxman A, Marchevsky NG, Jenkin D, Aboagye J, Aley PK, Angus B, | |
et al. Reactogenicity and immunogenicity after a late second dose or a | |
third dose of ChAdOx1 nCoV-19 in the UK: a substudy of two randomized | |
controlled trials (COV001 and COV002). Lancet 2021;398(10304):981-90.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8409975</ArticleId> | |
<ArticleId IdType="pubmed">34480858</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Hsieh 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Hsieh SM, Liu WD, Huang YS, Lin YJ, Hsieh EF, Lian WC, et al. | |
Safety and immunogenicity of a recombinant stabilized prefusion | |
SARS-CoV-2 spike protein vaccine (MVC-COV1901) adjuvanted with CpG 1018 | |
and aluminum hydroxide in healthy adults: a phase 1, dose-escalation | |
study. eClinicalMedicine 2021;38:100989.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8233066</ArticleId> | |
<ArticleId IdType="pubmed">34222848</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Irfan 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Irfan N, Chagla Z. In South Africa, a 2-dose Oxford/AZ vaccine did | |
not prevent mild to moderate COVID-19 (cases mainly B.1.351 variant). | |
Annals of Internal Medicine 2021;174(5):JC50.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33939483</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Lazarus 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Lazarus R, Baos S, Cappel-Porter H, Carson-Stevens A, Clout M, | |
Culliford L, et al. The safety and immunogenicity of concomitant | |
administration of COVID-19 vaccines (ChAdOx1 or BNT162b2) with seasonal | |
influenza vaccines in adults: a phase IV, multicentre randomized | |
controlled trial with blinding (ComFluCOV). SSRN 2021 [Preprint]. [DOI: | |
10.2139/ssrn.3931758]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.2139/ssrn.3931758</ArticleId> | |
<ArticleId IdType="pmc">PMC8585490</ArticleId> | |
<ArticleId IdType="pubmed">34774197</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Patamatamkul 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Patamatamkul S, Thammawat S, Buranrat B. Induction of robust | |
neutralizing antibodies against the COVID-19 Delta variant with ChAdOx1 | |
nCoV-19 or BNT162b2 as a booster following a primary vaccination series | |
with CoronaVac. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.25.21264099]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.25.21264099</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ward 2021a {published data only}</Title> | |
<Reference> | |
<Citation>Ward BJ, Séguin A, Couillard J, Trépanier S, Landry N. | |
Phase III: randomized observer-blind trial to evaluate lot-to-lot | |
consistency of a new plant-derived quadrivalent virus like particle | |
influenza vaccine in adults 18-49 years of age. Vaccine | |
2021;39(10):1528-33.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33581920</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Wu 2021b {published data only}</Title> | |
<Reference> | |
<Citation>Wu K, Choi A, Koch M, Ma LZ, Hill A, Nunna N, et al. Preliminary | |
analysis of safety and immunogenicity of a SARS-CoV-2 variant vaccine | |
booster. medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.05.05.21256716]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.05.05.21256716</ArticleId> | |
<ArticleId IdType="pmc">PMC8604720</ArticleId> | |
<ArticleId IdType="pubmed">34526698</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zdanowski 2021 {published data only}</Title> | |
<Reference> | |
<Citation>Zdanowski W, Waśniewski T. Evaluation of SARS-CoV-2 spike | |
protein antibody titers in cord blood after COVID-19 vaccination during | |
pregnancy in Polish healthcare workers: preliminary results. Vaccines | |
2021;9(6):675.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8234119</ArticleId> | |
<ArticleId IdType="pubmed">34205434</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Additional references</Title> | |
<ReferenceList> | |
<Title>Abbasi 2020</Title> | |
<Reference> | |
<Citation>Abbasi J. COVID-19 and mRNA vaccines – first large test for | |
a new approach. JAMA 2020;324(12):1125-7.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">32880613</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Angkasekwinai 2022</Title> | |
<Reference> | |
<Citation>Angkasekwinai N, Sewatanon J, Niyomnaitham S, Phumiamorn S, | |
Sukapirom K, Sapsutthipas S, et al. Comparison of safety and | |
immunogenicity of CoronaVac and ChAdOx1 against the SARS-CoV-2 | |
circulating variants of concern (Alpha, Delta, Beta) in Thai healthcare | |
workers. Vaccine X 2022;10:100153.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8896862</ArticleId> | |
<ArticleId IdType="pubmed">35282410</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Attaway 2021</Title> | |
<Reference> | |
<Citation>Attaway AH, Scheraga RG, Bhimraj A, Biehl M, Hatipoğlu U. | |
Severe Covid-19 pneumonia: pathogenesis and clinical management. BMJ | |
2021;372:n436.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33692022</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Baden 2021</Title> | |
<Reference> | |
<Citation>Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et | |
al. Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. New England | |
Journal of Medicine 2021;384(5):403-16.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7787219</ArticleId> | |
<ArticleId IdType="pubmed">33378609</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Balduzzi 2019</Title> | |
<Reference> | |
<Citation>Balduzzi S, Rücker G, Schwarzer G. How to perform a | |
meta-analysis with R: a practical tutorial. Evidence-Based Mental Health | |
2019;22:153-60.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC10231495</ArticleId> | |
<ArticleId IdType="pubmed">31563865</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Borobia 2021</Title> | |
<Reference> | |
<Citation>Borobia AM, Carcas AJ, Pérez-Olmeda M, Castaño L, | |
Bertran MJ, García-Pérez J, et al. Immunogenicity and | |
reactogenicity of BNT162b2 booster in ChAdOx1-S-primed participants | |
(CombiVacS): a multicentre, open-label, randomised, controlled, phase 2 | |
trial. Lancet 2021;398(10295):121-30.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8233007</ArticleId> | |
<ArticleId IdType="pubmed">34181880</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Boutron 2020a</Title> | |
<Reference> | |
<Citation>Boutron I, Chaimani A, Meerpohl JJ, Hróbjartsson A, Devane D, | |
Rada G, et al. The COVID-NMA Project: building an evidence ecosystem for | |
the COVID-19 pandemic. Annals of Internal Medicine 2020;173(12):1015-7.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7518109</ArticleId> | |
<ArticleId IdType="pubmed">32931326</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Boutron 2020b</Title> | |
<Reference> | |
<Citation>Boutron I, Chaimani A, Meerpohl JJ, Hróbjartsson A, Devane D, | |
Rada G, et al. Interventions for preventing and treating COVID-19: | |
protocol for a living mapping of research and a living systematic | |
review. Cochrane Database of Systematic Reviews 2020, Issue 11. Art. No: | |
CD013769. [DOI: 10.1002/14651858.CD013769]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1002/14651858.CD013769</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Bucci 2021</Title> | |
<Reference> | |
<Citation>Bucci EM, Berkhof J, Gillibert A, Gopalakrishna G, Calogero RA, | |
Bouter LM, et al. Data discrepancies and substandard reporting of | |
interim data of Sputnik V phase 3 trial. Lancet 2021;397(10288):1881-3.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC9751705</ArticleId> | |
<ArticleId IdType="pubmed">33991475</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Bueno 2021</Title> | |
<Reference> | |
<Citation>Bueno SM, Abarca K, González PA, Gálvez NM, Soto JA, | |
Duarte LF, et al. Interim report: safety and immunogenicity of an | |
inactivated vaccine against SARS-CoV-2 in healthy Chilean adults in a | |
phase 3 clinical trial. medRxiv 2021 [Preprint].</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Cabanac 2021</Title> | |
<Reference> | |
<Citation>Cabanac G, Oikonomidi T, Boutron I. Day-to-day discovery of | |
preprint-publication links. Scientometrics 2021;126(6):5285-304.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8053368</ArticleId> | |
<ArticleId IdType="pubmed">33897069</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Castagneto Gissey 2021</Title> | |
<Reference> | |
<Citation>Castagneto Gissey L, Panunzi S, Maltese S, Russo MF, Angelini G, | |
De Gaetano A, et al. Living systematic meta-analysis of COVID-19 | |
vaccines and dose allocation strategies. SSRN  2021 [Preprint]. | |
[DOI: 10.2139/ssrn.3827806]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.2139/ssrn.3827806</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>CDC 2021</Title> | |
<Reference> | |
<Citation>Centers for Disease Control and Prevention. Understanding mRNA | |
COVID-19 vaccines. | |
www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/mrna.html | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Chaimani 2013</Title> | |
<Reference> | |
<Citation>Chaimani A, Higgins JP, Mavridis D, Spyridonos P, Salanti G. | |
Graphical tools for network meta-analysis in STATA. PLOS One  | |
2013;8 (10):e76654.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC3789683</ArticleId> | |
<ArticleId IdType="pubmed">24098547</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Chaimani 2015</Title> | |
<Reference> | |
<Citation>Chaimani A, Salanti G. Visualizing assumptions and results in | |
network meta-analysis: the Network Graphs Package. Stata Journal | |
2015;15(4):905-50.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Chaimani 2022</Title> | |
<Reference> | |
<Citation>Chaimani A, Caldwell DM, Li T, Higgins JP, Salanti G. Chapter 11: | |
Undertaking network meta-analyses. In: Higgins JP, Thomas J, Chandler J, | |
Cumpston M, Li T, Page MJ, Welch VA, editor(s). Cochrane Handbook for | |
Systematic Reviews of Interventions Version 6.3 (updated February 2022). | |
Cochrane, 2022. Available from training.cochrane.org/handbook.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Chappell 2021</Title> | |
<Reference> | |
<Citation>Chappell KJ, Mordant FL, Li Z, Wijesundara DK, Ellenberg P, | |
Lackenby JA, et al. Safety and immunogenicity of an MF59-adjuvanted | |
spike glycoprotein-clamp vaccine for SARS-CoV-2: a randomised, | |
double-blind, placebo-controlled, phase 1 trial. Lancet Infectious | |
Diseases 2021;21(10):1383-94.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8055208</ArticleId> | |
<ArticleId IdType="pubmed">33887208</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Che 2021</Title> | |
<Reference> | |
<Citation>Che Y, Liu X, Pu Y, Zhou M, Zhao Z, Jiang R, et al. Randomized, | |
double-blinded, placebo-controlled Phase 2 trial of an inactivated | |
severe acute respiratory syndrome coronavirus 2 vaccine in healthy | |
adults. Clinical Infectious Diseases 2021;73(11):e3949-55.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7717222</ArticleId> | |
<ArticleId IdType="pubmed">33165503</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Chu 2021</Title> | |
<Reference> | |
<Citation>Chu L, McPhee R, Huang W, Bennett H, Pajon R, Nestorova B, et al. | |
A preliminary report of a randomized controlled phase 2 trial of the | |
safety and immunogenicity of mRNA-1273 SARS-CoV-2 vaccine. Vaccine | |
2021;39(20):2791-9.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7871769</ArticleId> | |
<ArticleId IdType="pubmed">33707061</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Dal‐Ré 2021a</Title> | |
<Reference> | |
<Citation>Dal-Ré R, Bekker LG, Gluud C, Holm S, Jha V, Poland GA, et | |
al. Ongoing and future COVID-19 vaccine clinical trials: challenges and | |
opportunities. Lancet Infectious Diseases 2021;21(11):e342-7.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8131060</ArticleId> | |
<ArticleId IdType="pubmed">34019801</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Dal‐Ré 2021b</Title> | |
<Reference> | |
<Citation>Dal-Ré R, Orenstein W, Caplan AL. Being fair to participants | |
in placebo-controlled COVID-19 vaccine trials. Nature Medicine | |
2021;27(6):938.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33903751</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>DeZure 2016</Title> | |
<Reference> | |
<Citation>DeZure AD, Berkowitz NM, Graham BS, Ledgerwood JE. | |
Whole-inactivated and virus-like particle vaccine strategies for | |
chikungunya virus. Journal of Infectious Diseases 2016;214(Suppl | |
5):S497-9.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC5137244</ArticleId> | |
<ArticleId IdType="pubmed">27920180</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Dias 2010</Title> | |
<Reference> | |
<Citation>Dias S, Welton NJ, Caldwell DM, Ades AE. Checking consistency in | |
mixed treatment comparison meta-analysis. Statistics in Medicine | |
2010;29(7-8):932-44.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">20213715</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Dong 2020</Title> | |
<Reference> | |
<Citation>Dong Y, Dai T, Wei Y, Zhang L, Zheng M, Zhou F. A systematic | |
review of SARS-CoV-2 vaccine candidates. Signal Transduction and | |
Targeted Therapy 2020;5(1):237.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7551521</ArticleId> | |
<ArticleId IdType="pubmed">33051445</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Egger 1997</Title> | |
<Reference> | |
<Citation>Egger M, Smith GD, Schneider M, Minder C. Bias in meta-analysis | |
detected by a simple, graphical test. BMJ 1997;315:629-34.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC2127453</ArticleId> | |
<ArticleId IdType="pubmed">9310563</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ella 2020b</Title> | |
<Reference> | |
<Citation>Ella R, Reddy S, Jogdand H, Sarangi V, Ganneru B, Prasad S, et al. | |
Safety and immunogenicity clinical trial of an inactivated SARS-CoV-2 | |
vaccine, BBV152 (a phase 2, double-blind, randomised controlled trial) | |
and the persistence of immune responses from a phase 1 follow-up report. | |
medRxiv  2020 [Preprint]. [DOI: 10.1101/2020.12.21.20248643]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2020.12.21.20248643</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ella 2021a</Title> | |
<Reference> | |
<Citation>Ella R, Reddy S, Jogdand H, Sarangi V, Ganneru B, Prasad S, et al. | |
Safety and immunogenicity of an inactivated SARS-CoV-2 vaccine, BBV152: | |
interim results from a double-blind, randomized, multicentre, phase 2 | |
trial, and 3-month follow-up of a double-blind, randomized phase 1 | |
trial. Lancet Infectious Diseases 2021;21(7):950-61.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8221739</ArticleId> | |
<ArticleId IdType="pubmed">33705727</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Enjuanes 2016</Title> | |
<Reference> | |
<Citation>Enjuanes L, Zuñiga S, Castaño-Rodriguez C, | |
Gutierrez-Alvarez J, Canton J, Sola I. Molecular basis of coronavirus | |
virulence and vaccine development. Advances in Virus Research | |
2016;96:245-86.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7112271</ArticleId> | |
<ArticleId IdType="pubmed">27712626</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Epistemonikos</Title> | |
<Reference> | |
<Citation>Epistemonikos. Epistemonikos L·OVE COVID-19 platform. | |
Available at | |
app.iloveevidence.com/loves/5e6fdb9669c00e4ac072701d?utm=ile.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>FDA 2020a</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. Development and licensure of | |
vaccines to prevent COVID-19. Guidance for industry; June 2020. | |
www.fda.gov/media/139638/download (accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>FDA 2020b</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. FDA Briefing Document Moderna | |
COVID-19 Vaccine. Vaccines and Related Biological Products Advisory | |
Committee Meeting December 17, 2020. www.fda.gov/media/144434/download | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>FDA 2020c</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. FDA Briefing Document | |
Pfizer-BioNTech COVID-19 Vaccine. Vaccines and Related Biological | |
Products Advisory Committee Meeting December 10, 2020. | |
www.fda.gov/media/144245/download (accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>FDA 2021</Title> | |
<Reference> | |
<Citation>Food and Drug Administration. FDA Briefing Document Janssen | |
Ad26.COV2.S Vaccine for the Prevention of COVID-19. Vaccines and Related | |
Biological Products Advisory Committee Meeting February 26, 2021. | |
www.fda.gov/media/146217/download (accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Feikin 2022</Title> | |
<Reference> | |
<Citation>Feikin DR, Higdon MM, Abu-Raddad LJ, Andrews N, Araos R, Goldberg | |
Y, et al. Duration of effectiveness of vaccines against SARS-CoV-2 | |
infection and COVID-19 disease: results of a systematic review and | |
meta-regression. Lancet 2022;399(10328):924-44.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8863502</ArticleId> | |
<ArticleId IdType="pubmed">35202601</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Feng 2021</Title> | |
<Reference> | |
<Citation>Feng Y, Chen J, Yao T, Chang Y, Li X, Xing R, et al. Safety and | |
Immunogenicity of Inactivated SARS-CoV-2 vaccine in high-risk | |
occupational population: a randomized, parallel, controlled clinical | |
trial. medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.08.06.21261696]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.08.06.21261696</ArticleId> | |
<ArticleId IdType="pmc">PMC8692079</ArticleId> | |
<ArticleId IdType="pubmed">34933684</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Folegatti 2020</Title> | |
<Reference> | |
<Citation>Folegatti PM, Ewer KJ, Aley PK, Angus B, Becker S, | |
Belij-Rammerstorfer S, et al. Safety and immunogenicity of the ChAdOx1 | |
nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, | |
single-blind, randomised controlled trial. Lancet 2020;396:467-78.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7445431</ArticleId> | |
<ArticleId IdType="pubmed">32702298</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Formica 2021</Title> | |
<Reference> | |
<Citation>Formica N, Mallory R, Albert G, Robinson M, Plested JS, Cho I, et | |
al, the 2019nCoV-101 Study Group. Evaluation of a SARS-CoV-2 vaccine | |
NVX-CoV2373 in younger and older adults. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.02.26.21252482]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.02.26.21252482</ArticleId> | |
<ArticleId IdType="pmc">PMC8486115</ArticleId> | |
<ArticleId IdType="pubmed">34597298</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Fuenmayor 2017</Title> | |
<Reference> | |
<Citation>Fuenmayor J, Gòdia F, Cervera L. Production of virus-like | |
particles for vaccines. New Biotechnology 2017;39(Pt B):174-80.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7102714</ArticleId> | |
<ArticleId IdType="pubmed">28778817</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Gavi 2020</Title> | |
<Reference> | |
<Citation>Gavi. What are viral vector-based vaccines and how could they be | |
used against COVID-19? | |
www.gavi.org/vaccineswork/what-are-viral-vector-based-vaccines-and-how-could-they-be-used-against-covid-19 | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Gobeil 2021</Title> | |
<Reference> | |
<Citation>Gobeil P, Pillet S, Séguin A, Boulay I, Mahmood A, Vinh DC, | |
et al. Interim report of a Phase 2 randomized trial of a plant-produced | |
virus-like particle vaccine for Covid-19 in healthy adults aged 18-64 | |
and older adults aged 65 and older. medRxiv  2021 [Preprint]. [DOI: | |
10.1101/2021.05.14.21257248]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.05.14.21257248</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Goepfert 2021</Title> | |
<Reference> | |
<Citation>Goepfert PA, Fu B, Chabanon AL, Bonaparte MI, Davis MG, Essink BJ, | |
et al. Safety and immunogenicity of SARS-CoV-2 recombinant protein | |
vaccine formulations in healthy adults: interim results of a randomised, | |
placebo-controlled, phase 1-2, dose-ranging study. Lancet Infectious | |
Diseases 2021;21(9):1257-70.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8055206</ArticleId> | |
<ArticleId IdType="pubmed">33887209</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>GRADEpro GDT [Computer program]</Title> | |
<Reference> | |
<Citation>GRADEpro GDT. Version accessed 6 December 2021. Hamilton (ON): | |
McMaster University (developed by Evidence Prime). Available at | |
gradepro.org.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Guyatt 2011</Title> | |
<Reference> | |
<Citation>Guyatt GH, Oxman AD, Kunz R, Brozek J, Alonso-Coello P, Rind D, et | |
al. GRADE guidelines 6. Rating the quality of evidence – | |
imprecision. Journal of Clinical Epidemiology 2011;64(12):1283-93.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">21839614</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Harder 2021</Title> | |
<Reference> | |
<Citation>Harder T, Koch J, Vygen-Bonnet S, Kulper-Schiek W, Pilic A, Reda | |
S, et al. Efficacy and effectiveness of COVID-19 vaccines against | |
SARS-CoV-2 infection: interim results of a living systematic review, 1 | |
January to 14 May 2021. Eurosurveillance 2021;26(28):2100563.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8284046</ArticleId> | |
<ArticleId IdType="pubmed">34269175</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Hayawi 2021</Title> | |
<Reference> | |
<Citation>Hayawi K, Shahriar S, Serhani MA, Alashwal H, Masud MM. Vaccine | |
versus variants (3Vs): are the COVID-19 vaccines effective against the | |
variants? A systematic review. Vaccines 2021;9(11):1305.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8622454</ArticleId> | |
<ArticleId IdType="pubmed">34835238</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Heath 2021 </Title> | |
<Reference> | |
<Citation>Heath PT, Galiza EP, Baxter DN, Boffito M, Browne D, Burns F, et | |
al. Efficacy of the NVX-CoV2373 Covid-19 vaccine against the B.1.1.7 | |
variant. medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.05.13.21256639]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.05.13.21256639</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Higdon 2021</Title> | |
<Reference> | |
<Citation>Higdon MM, Wahl B, Jones CB, Rosen JG, Truelove SA, Baidya A, et | |
al. A systematic review of COVID-19 vaccine efficacy and effectiveness | |
against SARS-CoV-2 infection and disease. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.17.21263549]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.17.21263549</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Higgins 2021</Title> | |
<Reference> | |
<Citation>Higgins JP, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch | |
VA, editor(s). Cochrane Handbook for Systematic Reviews of Interventions | |
Version 6.2 (updated February 2021). Cochrane, 2021. Available from | |
training.cochrane.org/handbook/archive/v6.2.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Hobernik 2018</Title> | |
<Reference> | |
<Citation>Hobernik D, Bros M. DNA vaccines – how far from clinical | |
use? International Journal of Molecular Sciences 2018;19(11):3605.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC6274812</ArticleId> | |
<ArticleId IdType="pubmed">30445702</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Hultcrantz 2017</Title> | |
<Reference> | |
<Citation>Hultcrantz M, Rind D, Akl EA, Treweek S, Mustafa RA, Iorio A, et | |
al. The GRADE Working Group clarifies the construct of certainty of | |
evidence. Journal of Clinical Epidemiology 2017;87:4-13.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC6542664</ArticleId> | |
<ArticleId IdType="pubmed">28529184</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Kirkham 2018</Title> | |
<Reference> | |
<Citation>Kirkham JJ, Altman DG, Chan AW, Gamble C, Dwan KM, Williamson PR. | |
Outcome reporting bias in trials: a methodological approach for | |
assessment and adjustment in systematic reviews. BMJ 2018;362:k3802.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC6161807</ArticleId> | |
<ArticleId IdType="pubmed">30266736</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Korang 2022</Title> | |
<Reference> | |
<Citation>Korang SK, Rohden E, Veroniki AA, Ong G, Ngalamika O, Siddiqui F, | |
et al. Vaccines to prevent COVID-19: a living systematic review with | |
trial sequential analysis and network meta-analysis of randomized | |
clinical trials. PLOS One 2022;17(1):e0260733.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8782520</ArticleId> | |
<ArticleId IdType="pubmed">35061702</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Kow 2022</Title> | |
<Reference> | |
<Citation>Kow CS, Ramachandram DS, Hasan SS. The effectiveness of mRNA-1273 | |
vaccine against COVID-19 caused by Delta variant: a systematic review | |
and meta-analysis. Journal of Medical Virology 2022;94(5):2269-74.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC9015635</ArticleId> | |
<ArticleId IdType="pubmed">34978339</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Lazarus 2021</Title> | |
<Reference> | |
<Citation>Lazarus R, Taucher C, Brown C, Čorbic I, Danon L, Dubischar | |
K, et al. Immunogenicity and safety of inactivated whole virion | |
Coronavirus vaccine with CpG (VLA2001) in healthy adults aged 18 to 55: | |
a randomised phase 1 /2 clinical trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.08.13.21262021]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.08.13.21262021</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Li 2021b</Title> | |
<Reference> | |
<Citation>Li J, Hui A, Zhang X, Yang Y, Tang R, Ye H, et al. Safety and | |
immunogenicity of the SARS-CoV-2 BNT162b1 mRNA vaccine in younger and | |
older Chinese adults: a randomized, placebo-controlled, double-blind | |
phase 1 study. Nature Medicine 2021;27(6):1062-70.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33888900</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Li 2021c</Title> | |
<Reference> | |
<Citation>Li M, Yang J, Wang L, Wu Q, Wu Z, Zheng W, et al. A booster dose | |
is immunogenic and will be needed for older adults who have completed | |
two doses vaccination with CoronaVac: a randomized, double-blind, | |
placebo-controlled, phase 1/2 clinical trial. medRxiv 2021 [Preprint]. | |
[DOI: 10.1101/2021.08.03.21261544]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.08.03.21261544</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Liu 2021</Title> | |
<Reference> | |
<Citation>Liu X, Shaw RH, Stuart AS, Greenland M, Dinesh T, | |
Provstgaard-Morys S, et al. Safety and immunogenicity report from the | |
com-COV study – a single-blind randomised non-inferiority trial | |
comparing heterologous and homologous prime-boost schedules with an | |
adenoviral vectored and mRNA COVID-19 vaccine. SSRN 2021 [Preprint].</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8346248</ArticleId> | |
<ArticleId IdType="pubmed">34370971</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Low 2021</Title> | |
<Reference> | |
<Citation>Low JG, Alwis R, Chen S, Kalimuddin S, Leong YA, Mah TK, et al. A | |
phase 1/2 randomized, double-blinded, placebo controlled ascending dose | |
trial to assess the safety, tolerability and immunogenicity of ARCT-021 | |
in healthy adults. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.07.01.21259831]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.07.01.21259831</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Lv 2021</Title> | |
<Reference> | |
<Citation>Lv M, Luo X, Shen Q, Lei R, Liu X, Liu E, et al. Safety, | |
immunogenicity, and efficacy of COVID-19 vaccines in children and | |
adolescents: a systematic review. Vaccines 2021;9(10):1102.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8539812</ArticleId> | |
<ArticleId IdType="pubmed">34696210</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Madhi 2021</Title> | |
<Reference> | |
<Citation>Madhi SA, Koen AL, Fairlie L, Cutland CL, Baillie V, Padayachee | |
SD, et al. ChAdOx1 nCoV-19 (AZD1222) vaccine in people living with and | |
without HIV. Research Square 2021 [Preprint]. [DOI: | |
10.21203/rs.3.rs-322470/v1]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.21203/rs.3.rs-322470/v1</ArticleId> | |
<ArticleId IdType="pmc">PMC8372504</ArticleId> | |
<ArticleId IdType="pubmed">34416193</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Makris 2021</Title> | |
<Reference> | |
<Citation>Makris M, Pavord S, Lester W, Scully M, Hunt B. Vaccine-induced | |
immune thrombocytopenia and thrombosis (VITT). Research and Practice in | |
Thrombosis and Haemostasis 2021;5(5):e12529.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8178610</ArticleId> | |
<ArticleId IdType="pubmed">34136745</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Mammen 2021</Title> | |
<Reference> | |
<Citation>Mammen MP Jr, Tebas P, Agnes J, Giffear M, Kraynyak KA, Blackwood | |
E, et al. Safety and immunogenicity of INO-4800 DNA vaccine against | |
SARS-CoV-2: a preliminary report of a randomized, blinded, | |
placebo-controlled, Phase 2 clinical trial in adults at high risk of | |
viral exposure. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.05.07.21256652]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.05.07.21256652</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Marshall 2020</Title> | |
<Reference> | |
<Citation>Marshall JC, Murthy S, Diaz J, Adhikari NK, Angus DC, Arabi YM, et | |
al. A minimal common outcome measure set for COVID-19 clinical research. | |
Lancet Infectious Diseases 2020;20(8):e192-7.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7292605</ArticleId> | |
<ArticleId IdType="pubmed">32539990</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Mavridis 2014</Title> | |
<Reference> | |
<Citation>Mavridis D, Welton NJ, Sutton A, Salanti G. A selection model for | |
accounting for publication bias in a full network meta-analysis. | |
Statistics in Medicine 2014;33(30):5399-412.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">25316006</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Meng 2021b</Title> | |
<Reference> | |
<Citation>Meng FY, Gao F, Jia SY, Wu XH, Li JX, Guo XL, et al. Safety and | |
immunogenicity of a recombinant COVID-19 vaccine (Sf9 cells) in healthy | |
population aged 18 years or older: two single-center, randomised, | |
double-blind, placebo-controlled, phase 1 and phase 2 trials. Signal | |
Transduction and Targeted Therapy 2021;6(1):271.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8281021</ArticleId> | |
<ArticleId IdType="pubmed">34267185</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Mortola 2004</Title> | |
<Reference> | |
<Citation>Mortola E, Roy P. Efficient assembly and release of SARS | |
coronavirus-like particles by a heterologous expression system. FEBS | |
Letters 2004;576(1-2):174-8.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7126153</ArticleId> | |
<ArticleId IdType="pubmed">15474033</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Mulligan 2020</Title> | |
<Reference> | |
<Citation>Mulligan MJ, Lyke KE, Kitchin N, Absalon J, Gurtman A, Lockhart S, | |
et al. Phase I/II study of COVID-19 RNA vaccine BNT162b1 in adults. | |
Nature 2020;586(7830):589-93.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">32785213</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Nguyen 2021</Title> | |
<Reference> | |
<Citation>Nguyen TP, Do Q, Phan LT, Dinh DV, Khong H, Hoang LV, et al. | |
Safety and immunogenicity of Nanocovax, a SARS-CoV-2 recombinant spike | |
protein vaccine. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.07.22.21260942]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.07.22.21260942</ArticleId> | |
<ArticleId IdType="pmc">PMC9108376</ArticleId> | |
<ArticleId IdType="pubmed">35602004</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Nikolakopoulou 2020</Title> | |
<Reference> | |
<Citation>Nikolakopoulou A, Higgins JP, Papakonstantinou T, Chaimani A, Del | |
Giovane C, Egger M, et al. CINeMA: an approach for assessing confidence | |
in the results of a network meta-analysis. PLOS Medicine | |
2020;17 (4):e1003082.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7122720</ArticleId> | |
<ArticleId IdType="pubmed">32243458</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Oikonomidi 2020</Title> | |
<Reference> | |
<Citation>Oikonomidi T, Boutron I, Pierre O, Cabanac G, Ravaud P, COVID-19 | |
NMA Consortium. Changes in evidence for studies assessing interventions | |
for COVID-19 reported in preprints: meta-research study. BMC Medicine | |
2020;18(1):402.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7745199</ArticleId> | |
<ArticleId IdType="pubmed">33334338</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ostrowski 2021</Title> | |
<Reference> | |
<Citation>Ostrowski SR, Søgaard OS, Tolstrup M, Stærke NB, | |
Lundgren J, Østergaard L, et al. Inflammation and platelet | |
activation after COVID-19 vaccines – possible mechanisms behind | |
vaccine-induced immune thrombocytopenia and thrombosis. Frontiers in | |
Immunology 2021;12:779453.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8649717</ArticleId> | |
<ArticleId IdType="pubmed">34887867</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ouzzani 2016</Title> | |
<Reference> | |
<Citation>Ouzzani M, Hammady H, Fedorowicz Z, Elmagarmid A. Rayyanv – | |
a web and mobile app for systematic reviews. Systematic Reviews | |
2016;5(1):210.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC5139140</ArticleId> | |
<ArticleId IdType="pubmed">27919275</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Oxford Vaccine Group 2020</Title> | |
<Reference> | |
<Citation>Oxford Vaccine Group. Vaccine Knowledge Project: independent | |
information about vaccines and infectious diseases. vk.ovg.ox.ac.uk/vk | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Page 2021</Title> | |
<Reference> | |
<Citation>Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow | |
CD, et al. The PRISMA 2020 statement: an updated guideline for reporting | |
systematic reviews. BMJ 2021;372:n71.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8005924</ArticleId> | |
<ArticleId IdType="pubmed">33782057</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pajon 2021</Title> | |
<Reference> | |
<Citation>Pajon R, Paila YD, Girard B, Dixon G, Kacena K, Baden LR, et al. | |
Initial analysis of viral dynamics and circulating viral variants during | |
the mRNA-1273 Phase 3 COVE trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.28.21264252]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.28.21264252</ArticleId> | |
<ArticleId IdType="pmc">PMC9018421</ArticleId> | |
<ArticleId IdType="pubmed">35145311</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pan 2021a</Title> | |
<Reference> | |
<Citation>Pan HX, Liu JK, Huang BY, Li GF, Chang XY, Liu YF, et al. | |
Immunogenicity and safety of a SARS-CoV-2 inactivated vaccine (KCONVAC) | |
in healthy adults: two randomized, double-blind, and placebo-controlled | |
Phase 1/2 clinical trials. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.04.07.21253850]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.04.07.21253850</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pan 2021b</Title> | |
<Reference> | |
<Citation>Pan HX, Wu QH, Zeng G, Yang J, Jiang DY, Deng XW,  et al. | |
Immunogenicity and safety of a third dose, and immune persistence of | |
CoronaVac vaccine in healthy adults aged 18–59 years: interim | |
results from a double-blind, randomized, placebo-controlled phase 2 | |
clinical trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.07.23.21261026]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.07.23.21261026</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pérez‐Rodríguez 2021</Title> | |
<Reference> | |
<Citation>Pérez-Rodríguez S, la Caridad | |
Rodríguez-González M, Ochoa-Azze R, Climent-Ruiz Y, Alberto | |
González-Delgado C, Paredes-Moreno B, et al. A randomized, | |
double-blind phase I clinical trial of two recombinant dimeric RBD | |
COVID-19 vaccine candidates: safety, reactogenicity and immunogenicity. | |
medRxiv 2021 [Preprint]. [DOI: 10.1101/2021.10.04.21264522]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.10.04.21264522</ArticleId> | |
<ArticleId IdType="pmc">PMC8823954</ArticleId> | |
<ArticleId IdType="pubmed">35164986</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pitisuttithum 2021</Title> | |
<Reference> | |
<Citation>Pitisuttithum P, Luvira V, Lawpoolsri S, Muangnoicharoen S, | |
Kamolratanakul S, Sivakorn C, et al. Safety and immunogenicity of an | |
inactivated recombinant Newcastle disease virus vaccine expressing | |
SARS-CoV-2 spike: interim results of a randomised, placebo-controlled, | |
Phase 1/2 trial. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.17.21263758]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.17.21263758</ArticleId> | |
<ArticleId IdType="pmc">PMC8903824</ArticleId> | |
<ArticleId IdType="pubmed">35284808</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Polack 2020</Title> | |
<Reference> | |
<Citation>Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, | |
et al. Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. New | |
England Journal of Medicine 2020;383(27):2603-15.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7745181</ArticleId> | |
<ArticleId IdType="pubmed">33301246</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pollard 2021</Title> | |
<Reference> | |
<Citation>Pollard AJ, Bijker EM. A guide to vaccinology: from basic | |
principles to new developments. Nature Reviews Immunology | |
2021;21(2):83-100.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7754704</ArticleId> | |
<ArticleId IdType="pubmed">33353987</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Pu 2021</Title> | |
<Reference> | |
<Citation>Pu J, Yu Q, Yin Z, Zhang Y, Li X, Yin Q, et al. The safety and | |
immunogenicity of an inactivated SARS-CoV-2 vaccine in Chinese adults | |
aged 18–59 years: a phase I randomized, double-blinded, | |
controlled trial. Vaccine 2021;39(20):2746-54.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8040531</ArticleId> | |
<ArticleId IdType="pubmed">33875266</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Qiao 2020</Title> | |
<Reference> | |
<Citation>Qiao J. What are the risks of COVID-19 infection in pregnant | |
women? Lancet 2020;395(10226):760-2.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7158939</ArticleId> | |
<ArticleId IdType="pubmed">32151334</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ramasamy 2020</Title> | |
<Reference> | |
<Citation>Ramasamy MN, Minassian AM, Ewer KJ, Flaxman AL, Folegatti PM, | |
Owens DR, et al. Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine | |
administered in a prime-boost regimen in young and old adults (COV002): | |
a single-blind, randomized, controlled, phase 2/3 trial. Lancet | |
2020;396(10267):1979-93.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7674972</ArticleId> | |
<ArticleId IdType="pubmed">33220855</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Richmond 2021</Title> | |
<Reference> | |
<Citation>Richmond P, Hatchuel L, Dong M, Ma B, Hu B, Smolenov I, et al. | |
Safety and immunogenicity of S-Trimer (SCB-2019), a protein subunit | |
vaccine candidate for COVID-19 in healthy adults: a phase 1, randomized, | |
double-blind, placebo-controlled trial. Lancet 2021;397(10275):682-94.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7906655</ArticleId> | |
<ArticleId IdType="pubmed">33524311</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Riley 2011</Title> | |
<Reference> | |
<Citation>Riley RD, Higgins JP, Deeks JJ. Interpretation of random effects | |
meta-analyses. BMJ 2011;342:d549.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">21310794</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Rizk 2021</Title> | |
<Reference> | |
<Citation>Rizk JG, Gupta A, Sardar P, Henry BM, Lewin JC, Lippi G, et al. | |
Clinical characteristics and pharmacological management of COVID-19 | |
vaccine-induced immune thrombotic thrombocytopenia with cerebral venous | |
sinus thrombosis: a review. JAMA Cardiology 2021;6(12):1451-60.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">34374713</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Roozen 2021</Title> | |
<Reference> | |
<Citation>Roozen GV, Prins ML, Binnendijk R, den Hartog G, Kuiper VP, Prins | |
C, et al. Tolerability, safety and immunogenicity of intradermal | |
delivery of a fractional dose mRNA-1273 SARS-CoV-2 vaccine in healthy | |
adults as a dose sparing strategy. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.07.27.21261116]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.07.27.21261116</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Roper 2009</Title> | |
<Reference> | |
<Citation>Roper RL, Rehm KE. SARS vaccines: where are we? Expert Review of | |
Vaccines 2009;8(7):887-98.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7105754</ArticleId> | |
<ArticleId IdType="pubmed">19538115</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Rotshild 2021</Title> | |
<Reference> | |
<Citation>Rotshild V, Hirsh-Raccah B, Miskin I, Muszkat M, Matok I. | |
Comparing the clinical efficacy of COVID-19 vaccines: a systematic | |
review and network meta-analysis. Scientific Reports 2021;11(1):22777.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8611039</ArticleId> | |
<ArticleId IdType="pubmed">34815503</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Rubin 2013</Title> | |
<Reference> | |
<Citation>Rubin LG, Levin MJ, Ljungman P, Davies EG, Avery R, Tomblyn M, et | |
al. 2013 IDSA clinical practice guideline for vaccination of the | |
immunocompromized host. Clinical Infectious Diseases | |
2013;58(3):e44-e100.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">24311479</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Rucker 2013</Title> | |
<Reference> | |
<Citation>Rucker G, Schwarzer G, Rücker G, Schwarzer G, Krahn U, | |
König J. Network meta-analysis using frequentist methods – | |
package netmeta. cran.r–project.org (accessed prior to 1 November | |
2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ryzhikov 2021</Title> | |
<Reference> | |
<Citation>Ryzhikov AB, Ryzhikov ЕА, Bogryantseva MP, Usova SV, | |
Danilenko ED, Nechaeva EA, et al. A single blind, placebo-controlled | |
randomized study of the safety, reactogenicity and immunogenicity of the | |
"EpiVacCorona" vaccine for the prevention of COVID-19. Russian Journal | |
of Infection and Immunity 2021;11(2):283-96.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sadoff 2020c</Title> | |
<Reference> | |
<Citation>Sadoff J, Le Gars M, Shukarev G, Heerwegh D, Truyers C, Groot AM, | |
et al. Safety and immunogenicity of the Ad26. COV2. S COVID-19 vaccine | |
candidate: interim results of a phase 1/2a, double-blind, randomized, | |
placebo-controlled trial. MedRxiv 2020 [Preprint].</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Salanti 2011</Title> | |
<Reference> | |
<Citation>Salanti G, Ades AE, Ioannidis JP. Graphical methods and numerical | |
summaries for presenting results from multiple-treatment meta-analysis: | |
an overview and tutorial. Journal of Clinical Epidemiology | |
2011;64(2):163-7.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">20688472</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Schünemann 2021</Title> | |
<Reference> | |
<Citation>Schünemann HJ, Higgins JP, Vist GE, Glasziou P, Akl EA, | |
Skoetz N, et al. Chapter 14: Completing 'Summary of findings' tables and | |
grading the certainty of the evidence. In: Higgins JP, Thomas J, | |
Chandler J, Cumpston M, Li T, Page MJ, Welch VA, editor(s). Cochrane | |
Handbook for Systematic Reviews of Interventions Version 6.2 (updated | |
February 2021). Cochrane, 2021. Available from | |
training.cochrane.org/handbook/archive/v6.2.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sharifian‐Dorche 2021</Title> | |
<Reference> | |
<Citation>Sharifian-Dorche M, Bahmanyar M, Sharifian-Dorche A, Mohammadi P, | |
Nomovi M, Mowla A. Vaccine-induced immune thrombotic thrombocytopenia | |
and cerebral venous sinus thrombosis post COVID-19 vaccination; a | |
systematic review. Journal of the Neurological Sciences 2021;428:117607.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8330139</ArticleId> | |
<ArticleId IdType="pubmed">34365148</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Shinde 2021</Title> | |
<Reference> | |
<Citation>Shinde V, Bhikha S, Hoosain Z, Archary M, Bhorat Q, Fairlie L, et | |
al, for the 2019nCoV-501 Study Group. Preliminary efficacy of the | |
NVX-CoV2373 Covid-19 vaccine against the B.1.351 variant. medRxiv 2021 | |
[Preprint].</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8091623</ArticleId> | |
<ArticleId IdType="pubmed">33951374</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Shu 2021</Title> | |
<Reference> | |
<Citation>Shu YJ, He JF, Pei RJ, He P, Huang ZH, Chen SM, et al. | |
Immunogenicity and safety of a recombinant fusion protein vaccine (V-01) | |
against coronavirus disease 2019 in healthy adults: a randomized, | |
double-blind, placebo-controlled, phase II trial. Chinese Medical | |
Journal 2021;134(16):1967-76.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8382383</ArticleId> | |
<ArticleId IdType="pubmed">34310400</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sridhar 2021</Title> | |
<Reference> | |
<Citation>Sridhar S, Joaquin A, Bonaparte MI, Bueso A, Chabanon AL, Chen A, | |
et al. Safety and immunogenicity of a SARS-CoV-2 recombinant protein | |
vaccine with AS03 adjuvant in healthy adults: interim findings from a | |
phase 2, randomised, dose-finding, multi-centre study. medRxiv 2021 | |
[Preprint]. [DOI: 10.1101/2021.10.08.21264302]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.10.08.21264302</ArticleId> | |
<ArticleId IdType="pmc">PMC8789245</ArticleId> | |
<ArticleId IdType="pubmed">35090638</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Stephenson 2021</Title> | |
<Reference> | |
<Citation>Stephenson KE, Le Gars M, Sadoff J, Groot AM, Heerwegh D, Truyers | |
C, et al. Immunogenicity of the Ad26.COV2.S vaccine for COVID-19. JAMA | |
2021;325(15):1535-44.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7953339</ArticleId> | |
<ArticleId IdType="pubmed">33704352</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Sterne 2019</Title> | |
<Reference> | |
<Citation>Sterne JA, Savović J, Page MJ, Elbers RG, Blencowe NS, | |
Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in | |
randomized trials. BMJ 2019;366:l4898.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">31462531</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Thomas 2021</Title> | |
<Reference> | |
<Citation>Thomas SJ, Moreira ED, Kitchin N, Absalon J, Gurtman A, Lockhart | |
S, et al. Six month safety and efficacy of the BNT162b2 Mrna Covid-19 | |
vaccine. medRxiv 2021 [Preprint].</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8461570</ArticleId> | |
<ArticleId IdType="pubmed">34525277</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Turner 2012</Title> | |
<Reference> | |
<Citation>Turner RM, Davey J, Clarke MJ, Thompson SG, Higgins JP. Predicting | |
the extent of heterogeneity in meta-analysis, using empirical data from | |
the Cochrane Database of Systematic Reviews. International Journal of | |
Epidemiology 2012;41(3):818-27.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC3396310</ArticleId> | |
<ArticleId IdType="pubmed">22461129</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>van Riel 2020</Title> | |
<Reference> | |
<Citation>Riel D, Wit E. Next-generation vaccine platforms for COVID-19. | |
Nature Materials 2020;19(8):810-2.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">32704139</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Viechtbauer 2010</Title> | |
<Reference> | |
<Citation>Viechtbauer W. Conducting meta-analyses in R with the metafor | |
package. Journal of Statistical Software 2010;36(3):1-48.</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Voysey 2021b</Title> | |
<Reference> | |
<Citation>Voysey M, Costa Clemens SA, Madhi SA, Weckx LY, Folegatti PM, Aley | |
PK, et al. Single-dose administration and the influence of the timing of | |
the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 | |
(AZD1222) vaccine: a pooled analysis of four randomized trials. Lancet | |
2021;397(10277):881-91.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7894131</ArticleId> | |
<ArticleId IdType="pubmed">33617777</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Walsh 2021</Title> | |
<Reference> | |
<Citation>Walsh EE, Frenck R, Falsey AR, Kitchin N, Absalon J, Gurtman A, et | |
al. RNA-based COVID-19 vaccine BNT162b2 selected for a pivotal efficacy | |
study. medRxiv 2021 [Preprint].</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Ward 2021b</Title> | |
<Reference> | |
<Citation>Ward BJ, Gobeil P, Séguin A, Atkins J, Boulay I, Charbonneau | |
PY, et al. Phase 1 randomized trial of a plant-derived virus-like | |
particle vaccine for COVID-19. Nature Medicine 2021;27(6):1071-8.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8205852</ArticleId> | |
<ArticleId IdType="pubmed">34007070</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>White 2008</Title> | |
<Reference> | |
<Citation>White IR, Higgins JP, Wood AM. Allowing for uncertainty due to | |
missing data in meta-analysis – part 1: two-stage methods. | |
Statistics in Medicine 2008;27(5):711-27.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">17703496</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO 2020a</Title> | |
<Reference> | |
<Citation>World Health Organization. Coronavirus disease 2019 (COVID-19). | |
Situation report – 51. apps.who.int/iris/handle/10665/331475 | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO 2020b</Title> | |
<Reference> | |
<Citation>World Health Organization. Considerations for evaluation of | |
COVID19 vaccines. Points to consider for manufacturers of COVID-19 | |
vaccines. Version 24 September 2020. | |
www.who.int/docs/default-source/in-vitro-diagnostics/covid19/who-evaluation-covid-vaccine-w-lines.pdf?sfvrsn=701d3a65_2 | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO 2020c</Title> | |
<Reference> | |
<Citation>World Health Organization. WHO target product profiles for | |
COVID-19 vaccines. Version 3 – 29 April 2020. | |
www.who.int/docs/default-source/blue-print/who-target-product-profiles-for-covid-19-vaccines.pdf | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO 2022a</Title> | |
<Reference> | |
<Citation>World Health Organization. Tracking SARS-CoV-2 variants. | |
www.who.int/activities/tracking-SARS-CoV-2-variants (accessed prior to 1 | |
November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO 2022b</Title> | |
<Reference> | |
<Citation>World Health Organization. COVID-19 vaccine tracker and landscape. | |
www.who.int/publications/m/item/draft-landscape-of-covid-19-candidate-vaccines | |
(accessed prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>WHO Ad Hoc Expert Group 2021</Title> | |
<Reference> | |
<Citation>WHO Ad Hoc Expert Group on the Next Steps for Covid-19 Vaccine | |
Evaluation. Placebo-controlled trials of covid-19 vaccines – why | |
we still need them. New England Journal of Medicine 2021;384:e2. [DOI: | |
10.1056/NEJMp2033538]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1056/NEJMp2033538</ArticleId> | |
<ArticleId IdType="pubmed">33264543</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Worldometer 2022</Title> | |
<Reference> | |
<Citation>Worldometer. COVID-19 coronavirus pandemic. | |
www.worldometers.info/coronavirus/#countries (accessed prior to 1 | |
November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Wu 2021c</Title> | |
<Reference> | |
<Citation>Wu S, Huang J, Zhang Z, Wu J, Zhang J, Hu H, et al. Safety, | |
tolerability, and immunogenicity of an aerosolised adenovirus type-5 | |
vector-based COVID-19 vaccine (Ad5-nCoV) in adults: preliminary report | |
of an open-label and randomised phase 1 clinical trial. Lancet | |
Infectious Diseases 2021;21(12):1654-64.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8313090</ArticleId> | |
<ArticleId IdType="pubmed">34324836</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Xia 2020</Title> | |
<Reference> | |
<Citation>Xia S, Duan K, Zhang Y, Zhao D, Zhang H, Xie Z, et al. Effect of | |
an inactivated vaccine against SARS-CoV-2 on safety and immunogenicity | |
outcomes: interim analysis of 2 randomized clinical trials. JAMA | |
2020;324(10):951-60.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7426884</ArticleId> | |
<ArticleId IdType="pubmed">32789505</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Yang 2021</Title> | |
<Reference> | |
<Citation>Yang S, Li Y, Dai L, Wang J, He P, Li C, et al. Safety and | |
immunogenicity of a recombinant tandem-repeat dimeric RBD-based protein | |
subunit vaccine (ZF2001) against COVID-19 in adults: two randomized, | |
double-blind, placebo-controlled, phase 1 and 2 trials. Lancet | |
Infectious Diseases 2021;21(8):1107-19.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7990482</ArticleId> | |
<ArticleId IdType="pubmed">33773111</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Yepes‐Nuñez 2019</Title> | |
<Reference> | |
<Citation>Yepes-Nuñez JJ, Li SA, Guyatt G, Jack SM, Brozek JL, Beyene | |
J, et al. Development of the summary of findings table for network | |
meta-analysis. Journal of Clinical Epidemiology 2019;115:1-13.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">31055177</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zakarya 2021</Title> | |
<Reference> | |
<Citation>Zakarya K, Kutumbetov L, Orynbayev M, Abduraimov Y, Sultankulova | |
K, Kassenov M, et al. A single-centre, randomized, single-blind, | |
placebo-controlled phase 1 and an open-label phase 2 clinical trials | |
with a 6 months follow-up in Kazakhstan. EClinicalMedicine | |
2021;39:101078.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8363482</ArticleId> | |
<ArticleId IdType="pubmed">34414368</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zeng 2021a</Title> | |
<Reference> | |
<Citation>Zeng L, Brignardello-Petersen R, Hultcrantz M, Siemieniuk RA, | |
Santesso N, Traversy G, et al. GRADE guidelines 32: GRADE offers | |
guidance on choosing targets of GRADE certainty of evidence ratings. | |
Journal of Clinical Epidemiology 2021;137:163-75.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pubmed">33857619</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zeng 2021b</Title> | |
<Reference> | |
<Citation>Zeng B, Gao L, Zhou Q, Yu K, Sun F. Effectiveness of COVID-19 | |
vaccines against SARS-CoV-2 variants of concern: a systematic review and | |
meta-analysis. medRxiv 2021 [Preprint]. [DOI: | |
10.1101/2021.09.23.21264048]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1101/2021.09.23.21264048</ArticleId> | |
<ArticleId IdType="pmc">PMC9126103</ArticleId> | |
<ArticleId IdType="pubmed">35606843</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zhang 2021b</Title> | |
<Reference> | |
<Citation>Zhang J, Hu Z, He J, Liao Y, Li Y, Pei R, et al. Safety and | |
immunogenicity of a recombinant interferon-armed RBD dimer vaccine | |
(V-01) for COVID-19 in healthy adults: a randomized, double-blind, | |
placebo-controlled, Phase I trial. Emerging Microbes & Infections | |
2021;10(1):1589-97.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8366678</ArticleId> | |
<ArticleId IdType="pubmed">34197281</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zhu 2020</Title> | |
<Reference> | |
<Citation>Zhu FC, Guan XH, Li YH, Huang JY, Jiang T, Hou LH, et al. | |
Immunogenicity and safety of a recombinant adenovirus type-5-vectored | |
COVID-19 vaccine in healthy adults aged 18 years or older: a randomized, | |
double-blind, placebo-controlled, phase 2 trial. Lancet | |
2020;396(10249):479-88.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC7836858</ArticleId> | |
<ArticleId IdType="pubmed">32702299</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zhu 2021a</Title> | |
<Reference> | |
<Citation>Zhu F, Jin P, Zhu T, Wang W, Ye H, Pan H, et al. Safety and | |
immunogenicity of a recombinant adenovirus type-5-vectored COVID-19 | |
vaccine with a homologous prime-boost regimen in healthy participants | |
aged 6 years and above: a randomized, double-blind, placebo-controlled, | |
phase 2b trial. Clinical Infectious Diseases 2022;75(1):e783-91. [DOI: | |
10.1093/cid/ciab845]</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="doi">10.1093/cid/ciab845</ArticleId> | |
<ArticleId IdType="pmc">PMC8522421</ArticleId> | |
<ArticleId IdType="pubmed">34551104</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>Zhu 2022</Title> | |
<Reference> | |
<Citation>Zhu F, Jin P, Zhu T, Wang W, Ye H, Pan H, et al. Safety and | |
immunogenicity of a recombinant adenovirus type-5-vectored COVID-19 | |
vaccine with a homologous prime-boost regimen in healthy participants | |
aged 6 years and above: a randomized, double-blind, placebo-controlled, | |
phase 2b trial. Clinical Infectious Diseases 2022;75(1):e783-91.</Citation> | |
<ArticleIdList> | |
<ArticleId IdType="pmc">PMC8522421</ArticleId> | |
<ArticleId IdType="pubmed">34551104</ArticleId> | |
</ArticleIdList> | |
</Reference> | |
</ReferenceList> | |
</ReferenceList> | |
<ReferenceList> | |
<Title>References to other published versions of this review</Title> | |
<ReferenceList> | |
<Title>Grana 2021</Title> | |
<Reference> | |
<Citation>Grana C, Ghosn L, Boutron I. Efficacy and safety of COVID-19 | |
vaccines: a systematic review and meta-analysis. PROSPERO 2021 | |
CRD42021271897. | |
www.crd.york.ac.uk/prospero/display_record.php?RecordID=271897 (accessed | |
prior to 1 November 2022).</Citation> | |
</Reference> | |
</ReferenceList> | |
</ReferenceList> | |
</PubmedData> | |
</PubmedArticle> | |
</PubmedArticleSet> |