Neutralizing antibodies for the prevention and treatment of COVID-19

被引:90
|
作者
Du, Lanying [1 ]
Yang, Yang [2 ]
Zhang, Xiujuan [1 ]
机构
[1] New York Blood Ctr, Lindsley F Kimball Res Inst, New York, NY 10021 USA
[2] Iowa State Univ, Roy J Carver Dept Biochem Biophys & Mol Biol, Ames, IA USA
关键词
SARS-CoV-2; Spike protein; Neutralization; Monoclonal antibodies; COVID-19; RECEPTOR-BINDING DOMAIN; PRACTICES INTERIM RECOMMENDATION; SARS-COV-2; SPIKE; ADVISORY-COMMITTEE; UNITED-STATES; MONOCLONAL-ANTIBODIES; PROTEIN; VACCINE; IDENTIFICATION; MUTATIONS;
D O I
10.1038/s41423-021-00752-2
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) initiates the infection process by binding to the viral cellular receptor angiotensin-converting enzyme 2 through the receptor-binding domain (RBD) in the S1 subunit of the viral spike (S) protein. This event is followed by virus-cell membrane fusion mediated by the S2 subunit, which allows virus entry into the host cell. Therefore, the SARS-CoV-2 S protein is a key therapeutic target, and prevention and treatment of coronavirus disease 2019 (COVID-19) have focused on the development of neutralizing monoclonal antibodies (nAbs) that target this protein. In this review, we summarize the nAbs targeting SARS-CoV-2 proteins that have been developed to date, with a focus on the N-terminal domain and RBD of the S protein. We also describe the roles that binding affinity, neutralizing activity, and protection provided by these nAbs play in the prevention and treatment of COVID-19 and discuss the potential to improve nAb efficiency against multiple SARS-CoV-2 variants. This review provides important information for the development of effective nAbs with broad-spectrum activity against current and future SARS-CoV-2 strains.
引用
收藏
页码:2293 / 2306
页数:14
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