Broadly neutralizing antibodies to SARS-CoV-2 and other human coronaviruses

被引:234
作者
Chen, Yanjia [1 ]
Zhao, Xiaoyu [1 ]
Zhou, Hao [2 ,3 ]
Zhu, Huanzhang [1 ]
Jiang, Shibo [4 ]
Wang, Pengfei [1 ]
机构
[1] Fudan Univ, Sch Life Sci, Shanghai Inst Infect Dis & Biosecur, State Key Lab Genet Engn, Shanghai, Peoples R China
[2] NYU, Grossman Sch Med, Dept Microbiol, 550 1St Ave, New York, NY 10003 USA
[3] Chengdu Univ Tradit Chinese Med, Coll Med Technol, Chengdu, Peoples R China
[4] Fudan Univ, Sch Basic Med Sci, Shanghai Inst Infect Dis & Biosecur, Key Lab Med Mol Virol MOE NHC CAMS, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
MONOCLONAL-ANTIBODIES; VARIANTS; INSIGHTS; SARS;
D O I
10.1038/s41577-022-00784-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines. The ancestral strain of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into a number of variants of concern. In this Review, Wang and colleagues discuss progress in the development and characterization of broadly neutralizing antibodies to SARS-CoV-2, which may lead to new antibody therapeutics and inform the design of next-generation vaccines.
引用
收藏
页码:189 / 199
页数:11
相关论文
共 106 条
[1]   Antibody evasion of SARS-CoV-2 Omicron BA.1, BA.1.1, BA.2, and BA.3 sub-lineages [J].
Ai, Jingwen ;
Wang, Xun ;
He, Xinyi ;
Zhao, Xiaoyu ;
Zhang, Yi ;
Jiang, Yuchao ;
Li, Minghui ;
Cui, Yuchen ;
Chen, Yanjia ;
Qiao, Rui ;
Li, Lin ;
Yang, Lulu ;
Li, Yi ;
Hu, Zixin ;
Zhang, Wenhong ;
Wang, Pengfei .
CELL HOST & MICROBE, 2022, 30 (08) :1077-+
[2]   The Humoral Response to HIV-1: New Insights, Renewed Focus [J].
Alter, Galit ;
Moody, M. Anthony .
JOURNAL OF INFECTIOUS DISEASES, 2010, 202 :S315-S322
[3]  
Annavajhala MK, 2021, NATURE, V597, P703, DOI [10.1101/2021.02.23.21252259, 10.1038/s41586-021-03908-2]
[4]  
Banach BB, 2021, CELL REP, V37, DOI [10.1016/j.celrep.2021.109771, 10.1101/2020.12.31.424987]
[5]   SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies [J].
Barnes, Christopher O. ;
Jette, Claudia A. ;
Abernathy, Morgan E. ;
Dam, Kim-Marie A. ;
Esswein, Shannon R. ;
Gristick, Harry B. ;
Malyutin, Andrey G. ;
Sharaf, Naima G. ;
Huey-Tubman, Kathryn E. ;
Lee, Yu E. ;
Robbiani, Davide F. ;
Nussenzweig, Michel C. ;
West, Anthony P., Jr. ;
Bjorkman, Pamela J. .
NATURE, 2020, 588 (7839) :682-+
[6]   SARS-CoV-2 infects cells after viral entry via clathrin-mediated endocytosis [J].
Bayati, Armin ;
Kumar, Rahul ;
Francis, Vincent ;
McPherson, Peter S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2021, 296
[7]   TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells [J].
Bestle, Dorothea ;
Heindl, Miriam Ruth ;
Limburg, Hannah ;
Thuy Van Lam Van ;
Pilgram, Oliver ;
Moulton, Hong ;
Stein, David A. ;
Hardes, Kornelia ;
Eickmann, Markus ;
Dolnik, Olga ;
Rohde, Cornelius ;
Klenk, Hans-Dieter ;
Garten, Wolfgang ;
Steinmetzer, Torsten ;
Boettcher-Friebertshaeuser, Eva .
LIFE SCIENCE ALLIANCE, 2020, 3 (09)
[8]  
Cameroni E, 2022, NATURE, V602, P664, DOI [10.1038/s41586-021-04386-2, 10.1101/2021.12.12.472269]
[9]  
Cao Y, 2022, bioRxiv, DOI [10.1101/2022.07.18.500332, 10.1101/2022.07.18.500332, DOI 10.1101/2022.07.18.500332]
[10]   BA.2.12.1, BA.4 and BA.5 escape antibodies elicited by Omicron infection [J].
Cao, Yunlong ;
Yisimayi, Ayijiang ;
Jian, Fanchong ;
Song, Weiliang ;
Xiao, Tianhe ;
Wang, Lei ;
Du, Shuo ;
Wang, Jing ;
Li, Qianqian ;
Chen, Xiaosu ;
Yu, Yuanling ;
Wang, Peng ;
Zhang, Zhiying ;
Liu, Pulan ;
An, Ran ;
Hao, Xiaohua ;
Wang, Yao ;
Feng, Rui ;
Sun, Haiyan ;
Zhao, Lijuan ;
Zhang, Wen ;
Zhao, Dong ;
Zheng, Jiang ;
Yu, Lingling ;
Li, Can ;
Zhang, Na ;
Wang, Rui ;
Niu, Xiao ;
Yang, Sijie ;
Song, Xuetao ;
Chai, Yangyang ;
Hu, Ye ;
Shi, Yansong ;
Zheng, Linlin ;
Li, Zhiqiang ;
Gu, Qingqing ;
Shao, Fei ;
Huang, Weijin ;
Jin, Ronghua ;
Shen, Zhongyang ;
Wang, Youchun ;
Wang, Xiangxi ;
Xiao, Junyu ;
Xie, Xiaoliang Sunney .
NATURE, 2022, 608 (7923) :593-+