Broad strategies for neutralizing SARS-CoV-2 and other human coronaviruses with monoclonal antibodies

被引:0
|
作者
Zhiyang Ling [1 ,2 ]
Chunyan Yi [1 ,2 ]
Xiaoyu Sun [1 ,2 ]
Zhuo Yang [1 ,2 ]
Bing Sun [1 ,2 ,3 ]
机构
[1] State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science,Chinese Academy of Sciences
[2] University of Chinese Academy of Sciences
[3] School of Life Science and Technology, Shanghai Tech University
基金
中国国家自然科学基金;
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D O I
暂无
中图分类号
R392-33 [免疫学技术、设备及实验方法];
学科分类号
摘要
Antibody therapeutics and vaccines for coronavirus disease 2019(COVID-19) have been approved in many countries, with most being developed based on the original strain of severe acute respiratory syndrome coronavirus 2(SARS-Co V-2). SARS-Co V-2has an exceptional ability to mutate under the pressure of host immunity, especially the immune-dominant spike protein of the virus, which is the target of both antibody drugs and vaccines. Given the continuous evolution of the virus and the identification of critical mutation sites, the World Health Organization(WHO) has named 5 variants of concern(VOCs): 4 are previously circulating VOCs, and 1 is currently circulating(Omicron). Due to multiple mutations in the spike protein, the recently emerged Omicron and descendent lineages have been shown to have the strongest ability to evade the neutralizing antibody(NAb) effects of current antibody drugs and vaccines. The development and characterization of broadly neutralizing antibodies(b NAbs) will provide broad strategies for the control of the sophisticated virus SARS-Co V-2. In this review, we describe how the virus evolves to escape NAbs and the potential neutralization mechanisms that associated with b NAbs. We also summarize progress in the development of b NAbs against SARS-Co V-2, human coronaviruses(Co Vs) and other emerging pathogens and highlight their scientific and clinical significance.
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页码:658 / 678
页数:21
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