SARS-CoV-2 spike S2-specific neutralizing antibodies

被引:23
作者
Li, Chia-Jung [1 ]
Chang, Shih-Chung [1 ,2 ,3 ,4 ]
机构
[1] Natl Taiwan Univ, Coll Life Sci, Dept Biochem Sci & Technol, Taipei, Taiwan
[2] Natl Taiwan Univ, Ctr Biotechnol, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Life Sci, Dept Biochem Sci & Technol, Taipei 106, Taiwan
[4] Natl Taiwan Univ, Ctr Biotechnol, Taipei 106, Taiwan
关键词
SARS-CoV-2; spike protein; S2; subunit; neutralizing antibody; antibody cocktail therapy;
D O I
10.1080/22221751.2023.2220582
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since the onset of the coronavirus disease 2019 (COVID-19), numerous neutralizing antibodies (NAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been developed and authorized for emergency use to control the pandemic. Most COVID-19 therapeutic NAbs prevent the S1 subunit of the SARS-CoV-2 spike (S) protein from binding to the human host receptor. However, the emergence of SARS-CoV-2 immune escape variants, which possess frequent mutations on the S1 subunit, may render current NAbs ineffective. In contrast, the relatively conserved S2 subunit of the S protein can elicit NAbs with broader neutralizing potency against various SARS-CoV-2 variants. In this review, the binding specificity and functional features of SARS-CoV-2 NAbs targeting different domains of the S2 subunit are collectively discussed. The knowledge learned from the investigation of the S2-specific NAbs provides insights and potential strategies for developing antibody cocktail therapy and next-generation coronavirus vaccine.
引用
收藏
页数:14
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