Three epitope-distinct human antibodies from RenMab mice neutralize SARS-CoV-2 and cooperatively minimize the escape of mutants

被引:13
|
作者
Nie, Jianhui [1 ,2 ]
Xie, Jingshu [3 ]
Liu, Shuo [1 ,2 ]
Wu, Jiajing [1 ,2 ]
Liu, Chuan [4 ]
Li, Jianhui [3 ]
Liu, Yacui [3 ]
Wang, Meiyu [1 ,2 ]
Zhao, Huizhen [3 ]
Zhang, Yabo [3 ]
Yao, Jiawei [3 ]
Chen, Lei [3 ]
Shen, Yuelei [3 ]
Yang, Yi [3 ]
Wang, Hong-Wei [5 ]
Wang, Youchun [1 ,2 ]
Huang, Weijin [1 ,2 ]
机构
[1] Natl Inst Food & Drug Control NIFDC, Div HIV AIDS & Sextransmitted Virus Vaccines, Inst Biol Product Control, Beijing, Peoples R China
[2] WHO Collaborating Ctr Stand & Evaluat Biol, Beijing, Peoples R China
[3] Beijing Biocytogen Co Ltd, Beijing, Peoples R China
[4] Shuimu BioSci Co Ltd, Beijing, Peoples R China
[5] Tsinghua Univ, Minist Educ, Key Lab Prot Sci,Sch Life Sci, Tsinghua Peking Joint Ctr Life Sci,Beijing Adv In, Beijing, Peoples R China
基金
比尔及梅琳达.盖茨基金会; 中国国家自然科学基金;
关键词
MUTATIONS; SPIKE;
D O I
10.1038/s41421-021-00292-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Coronavirus disease 2019 (COVID-19), a pandemic disease caused by the newly emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused more than 3.8 million deaths to date. Neutralizing antibodies are effective therapeutic measures. However, many naturally occurring mutations at the receptor-binding domain (RBD) have emerged, and some of them can evade existing neutralizing antibodies. Here, we utilized RenMab, a novel mouse carrying the entire human antibody variable region, for neutralizing antibody discovery. We obtained several potent RBD-blocking antibodies and categorized them into four distinct groups by epitope mapping. We determined the involved residues of the epitope of three representative antibodies by cryo-electron microscopy (Cryo-EM) studies. Moreover, we performed neutralizing experiments with 50 variant strains with single or combined mutations and found that the mixing of three epitope-distinct antibodies almost eliminated the mutant escape. Our study provides a sound basis for the rational design of fully human antibody cocktails against SARS-CoV-2 and pre-emergent coronaviral threats.
引用
收藏
页数:11
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