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SARS-CoV-2 spike S2-specific neutralizing antibodies

期刊

EMERGING MICROBES & INFECTIONS
卷 12, 期 2, 页码 -

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TAYLOR & FRANCIS LTD
DOI: 10.1080/22221751.2023.2220582

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SARS-CoV-2; spike protein; S2 subunit; neutralizing antibody; antibody cocktail therapy

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Since the onset of COVID-19, numerous NAbs against SARS-CoV-2 have been developed, but the emergence of immune escape variants threatens their effectiveness. However, NAbs targeting the S2 subunit of the S protein may offer broader neutralizing potency. This review discusses the binding specificity and functional features of S2-specific NAbs, providing insights for antibody cocktail therapy and next-generation vaccines.
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.

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