Student Research Committee, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Rev Med Virol. 2022 Mar;32(2):e2277. doi: 10.1002/rmv.2277. Epub 2021 Jul 19.
BNT162b2 and mRNA-1273 are two types of mRNA-based vaccine platforms that have received emergency use authorization. The emergence of novel severe acute respiratory syndrome (SARS-CoV-2) variants has raised concerns of reduced sensitivity to neutralization by their elicited antibodies. We aimed to systematically review the most recent in vitro studies evaluating the effectiveness of BNT162b2 and mRNA-1273 induced neutralizing antibodies against SARS-CoV-2 variants of concern. We searched PubMed, Scopus, and Web of Science in addition to bioRxiv and medRxiv with terms including 'SARS-CoV-2', 'BNT162b2', 'mRNA-1273', and 'neutralizing antibody' up to June 29, 2021. A modified version of the Consolidated Standards of Reporting Trials (CONSORT) checklist was used for assessing included study quality. A total 36 in vitro studies meeting the eligibility criteria were included in this systematic review. B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma), and B.1.617.2 (Delta) are four SARS-CoV-2 variants that have recently been identified as variants of concern. Included studies implemented different methods regarding pseudovirus or live virus neutralization assays for measuring neutralization titres against utilized viruses. After two dose vaccination by BNT162b2 or mRNA-1273, the B.1.351 variant had the least sensitivity to neutralizing antibodies, while B.1.1.7 variant had the most sensitivity; that is, it was better neutralized relative to the comparator strain. P.1 and B.1.617.2 variants had an intermediate level of impaired naturalization activity of antibodies elicited by prior vaccination. Our review suggests that immune sera derived from vaccinated individuals might show reduced protection of individuals immunized with mRNA vaccines against more recent SARS-CoV-2 variants of concern.
BNT162b2 和 mRNA-1273 是两种已获得紧急使用授权的基于 mRNA 的疫苗平台。新型严重急性呼吸系统综合征 (SARS-CoV-2) 变体的出现引起了人们对其诱导的抗体中和敏感性降低的担忧。我们旨在系统地回顾最近评估 BNT162b2 和 mRNA-1273 诱导的中和抗体对关注的 SARS-CoV-2 变体的有效性的体外研究。我们在 2021 年 6 月 29 日之前,通过 PubMed、Scopus 和 Web of Science 以及 bioRxiv 和 medRxiv 搜索了包括“严重急性呼吸系统综合征 (SARS-CoV-2)”、“BNT162b2”、“mRNA-1273”和“中和抗体”等术语的研究。使用修改后的临床试验报告标准 (CONSORT) 清单评估纳入研究的质量。本系统评价共纳入 36 项符合入选标准的体外研究。B.1.1.7 (Alpha)、B.1.351 (Beta)、P.1 (Gamma) 和 B.1.617.2 (Delta) 是最近被确定为关注变体的四种 SARS-CoV-2 变体。纳入的研究采用了不同的方法,包括假病毒或活病毒中和测定法,用于测量针对所使用病毒的中和滴度。接种两剂 BNT162b2 或 mRNA-1273 后,B.1.351 变体对中和抗体的敏感性最低,而 B.1.1.7 变体的敏感性最高;也就是说,相对于比较株,它被更好地中和。P.1 和 B.1.617.2 变体的抗体自然化活性受损程度处于中间水平。我们的综述表明,来自接种个体的免疫血清可能会降低先前接种 mRNA 疫苗的个体对更近期的 SARS-CoV-2 关注变体的保护。