Comparative systematic review and meta-analysis of reactogenicity, immunogenicity and efficacy of vaccines against SARS-CoV-2

被引:196
作者
McDonald, Ian [1 ]
Murray, Sam M. [1 ]
Reynolds, Catherine J. [1 ]
Altmann, Daniel M. [2 ]
Boyton, Rosemary J. [1 ,3 ]
机构
[1] Imperial Coll London, Fac Med, Dept Infect Dis, London, England
[2] Imperial Coll London, Fac Med, Dept Immunol & Inflammat, London, England
[3] Royal Brompton & Harefield Hosp, Lung Div, London, England
基金
英国医学研究理事会;
关键词
NEUTRALIZING ANTIBODY; HEALTHY-ADULTS; PROTECTIVE EFFICACY; IMMUNE-RESPONSES; SARS; CORONAVIRUS; COVID-19; SAFETY; ADENOVIRUS; MONKEYS;
D O I
10.1038/s41541-021-00336-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As SARS-CoV-2 vaccines are deployed worldwide, a comparative evaluation is important to underpin decision-making. We here report a systematic literature review and meta-analysis of Phase I/II/III human trials and non-human primates (NHP) studies, comparing reactogenicity, immunogenicity and efficacy across different vaccine platforms for comparative evaluation (updated to March 22, 2021). Twenty-three NHP and 32 human studies are included. Vaccines result in mostly mild, self-limiting adverse events. Highest spike neutralizing antibody (nAb) responses are identified for the mRNA-1273-SARS-CoV and adjuvanted NVX-CoV2373-SARS-CoV-2 vaccines. ChAdOx-SARS-CoV-2 produces the highest T cell ELISpot responses. Pre-existing nAb against vaccine viral vector are identified following AdH-5-SARS-CoV-2 vaccination, halving immunogenicity. The mRNA vaccines depend on boosting to achieve optimal immunogenicity especially in the elderly. BNT162b2, and mRNA-1273 achieve >94%, rAd26/5 > 91% and ChAdOx-SARS-CoV-2 > 66.7% efficacy. Across different vaccine platforms there are trade-offs between antibody binding, functional nAb titers, T cell frequency, reactogenicity and efficacy. Emergence of variants makes rapid mass rollout of high efficacy vaccines essential to reduce any selective advantage.
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页数:14
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