Potent neutralizing antibodies against multiple epitopes on SARS-CoV-2 spike

被引:939
|
作者
Liu, Lihong [1 ]
Wang, Pengfei [1 ]
Nair, Manoj S. [1 ]
Yu, Jian [1 ]
Rapp, Micah [2 ]
Wang, Qian [3 ]
Luo, Yang [1 ]
Chan, Jasper F-W [4 ,5 ]
Sahi, Vincent [1 ]
Figueroa, Amir [6 ]
Guo, Xinzheng, V [7 ]
Cerutti, Gabriele [2 ]
Bimela, Jude [2 ]
Gorman, Jason [8 ]
Zhou, Tongqing [8 ]
Chen, Zhiwei [4 ,5 ,9 ]
Yuen, Kwok-Yung [4 ,5 ]
Kwong, Peter D. [8 ,10 ]
Sodroski, Joseph G. [3 ]
Yin, Michael T. [11 ]
Sheng, Zizhang [1 ,2 ]
Huang, Yaoxing [1 ]
Shapiro, Lawrence [1 ,2 ,10 ]
Ho, David D. [1 ]
机构
[1] Columbia Univ, Vageros Coll Phys & Surg, Aaron Diamond AIDS Res Ctr, New York, NY 10027 USA
[2] Columbia Univ, Zuckerman Mind Brain Behav Inst, New York, NY 10027 USA
[3] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Univ Hong Kong, Li Ka Shing Fac Med, Carol Yu Ctr Infect, State Key Lab Emerging Infect Dis,Dept Microbiol, Hong Kong, Peoples R China
[5] Univ Hong Kong, Ctr Virol Vaccinol & Therapeut, Hlth InnoHK, Hong Kong, Peoples R China
[6] Columbia Univ, Dept Microbiol & Immunol, Vageros Coll Phys & Surg, Flow Cytometry Core, New York, NY USA
[7] Columbia Univ, Human Immune Monitoring Core, Vageros Coll Phys & Surg, New York, NY USA
[8] NIH, Vaccine Res Ctr, Bldg 10, Bethesda, MD 20892 USA
[9] Univ Hong Kong, Li Ka Shing Fac Med, AIDS Inst, Hong Kong, Peoples R China
[10] Columbia Univ, Dept Chem, New York, NY 10027 USA
[11] Columbia Univ, Dept Internal Med, Div Infect Dis, Vageros Coll Phys & Surg, New York, NY USA
关键词
CRYO-EM STRUCTURE; SARS CORONAVIRUS; VALIDATION; MODEL; VISUALIZATION; COMBINATION; OUTBREAK; PROTEIN; SEARCH;
D O I
10.1038/s41586-020-2571-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic continues, with devasting consequences for human lives and the global economy(1,2). The discovery and development of virus-neutralizing monoclonal antibodies could be one approach to treat or prevent infection by this coronavirus. Here we report the isolation of sixty-one SARS-CoV-2-neutralizing monoclonal antibodies from five patients infected with SARS-CoV-2 and admitted to hospital with severe coronavirus disease 2019 (COVID-19). Among these are nineteen antibodies that potently neutralized authentic SARS-CoV-2 in vitro, nine of which exhibited very high potency, with 50% virus-inhibitory concentrations of 0.7 to 9 ng ml(-1). Epitope mapping showed that this collection of nineteen antibodies was about equally divided between those directed against the receptor-binding domain (RBD) and those directed against the N-terminal domain (NTD), indicating that both of these regions at the top of the viral spike are immunogenic. In addition, two other powerful neutralizing antibodies recognized quaternary epitopes that overlap with the domains at the top of the spike. Cryo-electron microscopy reconstructions of one antibody that targets the RBD, a second that targets the NTD, and a third that bridges two separate RBDs showed that the antibodies recognize the closed, 'all RBD-down' conformation of the spike. Several of these monoclonal antibodies are promising candidates for clinical development as potential therapeutic and/or prophylactic agents against SARS-CoV-2. A diverse collection of potent neutralizing antibodies against the SARS-CoV-2 spike protein have been isolated from five patients with severe COVID-19 and high serum neutralization titres.
引用
收藏
页码:450 / +
页数:22
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