Identification of SARS-CoV RBD-targeting monoclonal antibodies with cross-reactive or neutralizing activity against SARS-CoV-2

被引:102
作者
Tai, Wanbo [1 ]
Zhang, Xiujuan [1 ]
He, Yuxian [2 ,3 ]
Jiang, Shibo [1 ,4 ]
Du, Lanying [1 ]
机构
[1] New York Blood Ctr, Lindsley F Kimball Res Inst, New York, NY 10065 USA
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, Beijing 100730, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Ctr AIDS Res, Beijing 100730, Peoples R China
[4] Fudan Univ, Sch Basic Med Sci, Key Lab Med Mol Virol MOE NHC CAMS, Shanghai 200032, Peoples R China
关键词
COVID-19; SARS-CoV-2; SARS-CoV; Receptor-binding domain; Neutralizing monoclonal antibodies; Cross-neutralization; RECEPTOR-BINDING DOMAIN; CORONAVIRUS SPIKE PROTEIN; PNEUMONIA OUTBREAK; EPITOPES; VACCINE; CHINA;
D O I
10.1016/j.antiviral.2020.104820
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SARS-CoV-2-caused COVID-19 cases are growing globally, calling for developing effective therapeutics to control the current pandemic. SARS-CoV-2 and SARS-CoV recognize angiotensin-converting enzyme 2 (ACE2) receptor via the receptor-binding domain (RBD). Here, we identified six SARS-CoV RBD-specific neutralizing monoclonal antibodies (nAbs) that cross-reacted with SARS-CoV-2 RBD, two of which, 18F3 and 7B11, neutralized SARS-CoV-2 infection. 18F3 recognized conserved epitopes on SARS-CoV and SARS-CoV-2 RBDs, whereas 7B11 recognized epitopes on SARS-CoV RBD not fully conserved in SARS-CoV-2 RBD. The 18F3-recognizing epitopes on RBD did not overlap with the ACE2-binding sites, whereas those recognized by 7B11 were close to the ACE2-binding sites, explaining why 7B11 could, but 18F3 could not, block SARS-CoV or SARS-CoV-2 RBD binding to ACE2 receptor. Our study provides an alternative approach to prevent SARS-CoV-2 infection using anti-SARS-CoV nAbs.
引用
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页数:6
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