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灭活疫苗诱导产生的强效抗体可以广泛中和流行的 SARS-CoV-2 变异株。

Inactivated vaccine-elicited potent antibodies can broadly neutralize SARS-CoV-2 circulating variants.

机构信息

Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing, 100084, China.

Institute of Infectious Diseases, Shenzhen Bay Laboratory, Shenzhen, Guangdong, 518132, China.

出版信息

Nat Commun. 2023 Apr 17;14(1):2179. doi: 10.1038/s41467-023-37926-7.

DOI:10.1038/s41467-023-37926-7
PMID:37069158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10107573/
Abstract

A full understanding of the inactivated COVID-19 vaccine-mediated antibody responses to SARS-CoV-2 circulating variants will inform vaccine effectiveness and vaccination development strategies. Here, we offer insights into the inactivated vaccine-induced antibody responses after prime-boost vaccination at both the polyclonal and monoclonal levels. We characterized the VDJ sequence of 118 monoclonal antibodies (mAbs) and found that 20 neutralizing mAbs showed varied potency and breadth against a range of variants including XBB.1.5, BQ.1.1, and BN.1. Bispecific antibodies (bsAbs) based on nonoverlapping mAbs exhibited enhanced neutralizing potency and breadth against the most antibody-evasive strains, such as XBB.1.5, BQ.1.1, and BN.1. The passive transfer of mAbs or their bsAb effectively protected female hACE2 transgenic mice from challenge with an infectious Delta or Omicron BA.2 variant. The neutralization mechanisms of these antibodies were determined by structural characterization. Overall, a broad spectrum of potent and distinct neutralizing antibodies can be induced in individuals immunized with the SARS-CoV-2 inactivated vaccine BBIBP-CorV, suggesting the application potential of inactivated vaccines and these antibodies for preventing infection by SARS-CoV-2 circulating variants.

摘要

全面了解针对 SARS-CoV-2 流行变异株的灭活 COVID-19 疫苗介导的抗体反应,将为疫苗效力和接种策略提供信息。在这里,我们从多克隆和单克隆水平深入了解了加强接种后的灭活疫苗诱导的抗体反应。我们对 118 株单克隆抗体(mAb)的 VDJ 序列进行了表征,发现 20 株中和 mAb 对包括 XBB.1.5、BQ.1.1 和 BN.1 在内的一系列变体表现出不同的效力和广度。基于非重叠 mAb 的双特异性抗体(bsAb)表现出针对最具抗体逃避能力的菌株(如 XBB.1.5、BQ.1.1 和 BN.1)的增强的中和效力和广度。mAb 或其 bsAb 的被动转移有效地保护了携带 hACE2 的雌性转基因小鼠免受传染性 Delta 或 Omicron BA.2 变体的挑战。通过结构特征来确定这些抗体的中和机制。总体而言,接种 SARS-CoV-2 灭活疫苗 BBIBP-CorV 的个体中可以诱导出广泛的、有效且独特的中和抗体,表明灭活疫苗和这些抗体在预防 SARS-CoV-2 流行变异株感染方面具有应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/b1f5a6fdfae4/41467_2023_37926_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/cc5deed6521b/41467_2023_37926_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/43410c9fceb2/41467_2023_37926_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/45fcf926eed0/41467_2023_37926_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/fb415d7ae921/41467_2023_37926_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/b1f5a6fdfae4/41467_2023_37926_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/cc5deed6521b/41467_2023_37926_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/43410c9fceb2/41467_2023_37926_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/45fcf926eed0/41467_2023_37926_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/fb415d7ae921/41467_2023_37926_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef62/10110575/b1f5a6fdfae4/41467_2023_37926_Fig5_HTML.jpg

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