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

Authors :
Yubin Liu
Ziyi Wang
Xinyu Zhuang
Shengnan Zhang
Zhicheng Chen
Yan Zou
Jie Sheng
Tianpeng Li
Wanbo Tai
Jinfang Yu
Yanqun Wang
Zhaoyong Zhang
Yunfeng Chen
Liangqin Tong
Xi Yu
Linjuan Wu
Dong Chen
Renli Zhang
Ningyi Jin
Weijun Shen
Jincun Zhao
Mingyao Tian
Xinquan Wang
Gong Cheng
Source :
Nature Communications, Vol 14, Iss 1, Pp 1-17 (2023)
Publication Year :
2023
Publisher :
Nature Portfolio, 2023.

Abstract

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.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.7bb4ce8f3e74d5bad738ec40b3dfe16
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-023-37926-7