The Assessment of Anti–SARS‐CoV‐2 Antibodies in Different Vaccine Platforms: A Systematic Review and Meta‐Analysis of COVID‐19 Vaccine Clinical Trial Studies

医学 荟萃分析 血清转化 大流行 2019年冠状病毒病(COVID-19) 安慰剂 疫苗试验 临床试验 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 内科学 抗体 病毒学 免疫学 替代医学 病理 传染病(医学专业) 疾病
作者
Mohammad Mirzakhani,Maryam Bayat,Mohammadreza Dashti,Safa Tahmasebi,Maryam Rostamtabar,Hadi Esmaeili Gouvarchin Ghaleh,Jafar Amani
出处
期刊:Reviews in Medical Virology [Wiley]
卷期号:34 (6)
标识
DOI:10.1002/rmv.2579
摘要

ABSTRACT Background and Objective The COVID‐19 pandemic spread rapidly throughout the world and caused millions of deaths globally. Several vaccines have been developed to control the COVID‐19 pandemic and reduce the burden it placed on public health. This study aimed to assess the efficacy of different vaccine platforms in inducing potent antibody responses. Moreover, the seroconversion rate and common side effects of vaccine platforms were evaluated. Methods This meta‐analysis included clinical trials of COVID‐19 vaccines that met the eligibility criteria. Electronic databases (including PubMed, Scopus, and Web of Science) and Google Scholar search engine were searched for eligible studies. Regarding the methodological heterogeneity between the included studies, we selected a random‐effects model. The geometric mean ratio (GMR) was chosen as the effect size for this meta‐analysis. Results Of the 1838 records identified through screening and after removing duplicate records, the full texts of 1076 records were assessed for eligibility. After the full‐text assessment, 56 records were eligible and included in the study. Overall, vaccinated participants had a 150.8‐fold increased rate of anti‐spike IgG titres compared with the placebo group (GMR = 150.8; 95% CI, 95.9–237.1; I 2 = 100%). Moreover, vaccinated participants had a 37.3‐fold increased rate of neutralising antibody titres compared with the placebo group (GMR = 37.3; 95% CI, 28.5–48.7; I 2 = 99%). The mRNA platform showed a higher rate of anti‐spike IgG (GMR = 1263.5; 95% CI, 431.1–3702.8; I 2 = 99%), while neutralising antibody titres were higher in the subunit platform (GMR = 53.4; 95% CI, 32.8–87.1; I 2 = 99%) than in other platforms. Different vaccine platforms showed different rates of both anti‐spike IgG and neutralising antibody titres with interesting results. The seroconversion rate of anti‐spike IgG and neutralising antibody titres was more than 98% in the vaccinated participants. Conclusion Inactivated and subunit vaccines produced a high percentage of neutralising antibodies and had a low common adverse reaction rate compared to other platforms. In this regard, subunit and inactivated vaccines can still be used as the main vaccine platforms for effectively controlling infections with high transmission rates.

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