A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection. Academic Article uri icon

Overview

abstract

  • Coronaviruses have caused several human epidemics and pandemics including the ongoing coronavirus disease 2019 (COVID-19). Prophylactic vaccines and therapeutic antibodies have already shown striking effectiveness against COVID-19. Nevertheless, concerns remain about antigenic drift in SARS-CoV-2 as well as threats from other sarbecoviruses. Cross-neutralizing antibodies to SARS-related viruses provide opportunities to address such concerns. Here, we report on crystal structures of a cross-neutralizing antibody, CV38-142, in complex with the receptor-binding domains from SARS-CoV-2 and SARS-CoV. Recognition of the N343 glycosylation site and water-mediated interactions facilitate cross-reactivity of CV38-142 to SARS-related viruses, allowing the antibody to accommodate antigenic variation in these viruses. CV38-142 synergizes with other cross-neutralizing antibodies, notably COVA1-16, to enhance neutralization of SARS-CoV and SARS-CoV-2, including circulating variants of concern B.1.1.7 and B.1.351. Overall, this study provides valuable information for vaccine and therapeutic design to address current and future antigenic drift in SARS-CoV-2 and to protect against zoonotic SARS-related coronaviruses.

publication date

  • April 15, 2021

Research

keywords

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • COVID-19
  • SARS-CoV-2
  • Severe Acute Respiratory Syndrome
  • Severe acute respiratory syndrome-related coronavirus

Identity

PubMed Central ID

  • PMC8049401

Scopus Document Identifier

  • 85105514394

Digital Object Identifier (DOI)

  • 10.1016/j.chom.2021.04.005

PubMed ID

  • 33894127

Additional Document Info

volume

  • 29

issue

  • 5