4.8 Article

Potent neutralizing antibodies against multiple epitopes on SARS-CoV-2 spike

Journal

NATURE
Volume 584, Issue 7821, Pages 450-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-020-2571-7

Keywords

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Funding

  1. Jack Ma Foundation
  2. JPB Foundation
  3. Tencent Charity Foundation
  4. NIH Common Fund Transformative High Resolution Cryo-Electron Microscopy program [U24 GM129539]
  5. Simons Foundation [SF349247]
  6. NY State Assembly
  7. NIH National Institute of General Medical Sciences [GM103310]
  8. Health@InnoHK (Centre for Virology, Vaccinology and Therapeutics), Innovation and Technology Commission, The Government of the Hong Kong Special Administrative Region
  9. Brii Biosciences
  10. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [ZIAAI005022, ZICAI005111, ZIAAI005147, ZIAAI005149] Funding Source: NIH RePORTER

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The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic continues, with devasting consequences for human lives and the global economy(1,2). The discovery and development of virus-neutralizing monoclonal antibodies could be one approach to treat or prevent infection by this coronavirus. Here we report the isolation of sixty-one SARS-CoV-2-neutralizing monoclonal antibodies from five patients infected with SARS-CoV-2 and admitted to hospital with severe coronavirus disease 2019 (COVID-19). Among these are nineteen antibodies that potently neutralized authentic SARS-CoV-2 in vitro, nine of which exhibited very high potency, with 50% virus-inhibitory concentrations of 0.7 to 9 ng ml(-1). Epitope mapping showed that this collection of nineteen antibodies was about equally divided between those directed against the receptor-binding domain (RBD) and those directed against the N-terminal domain (NTD), indicating that both of these regions at the top of the viral spike are immunogenic. In addition, two other powerful neutralizing antibodies recognized quaternary epitopes that overlap with the domains at the top of the spike. Cryo-electron microscopy reconstructions of one antibody that targets the RBD, a second that targets the NTD, and a third that bridges two separate RBDs showed that the antibodies recognize the closed, 'all RBD-down' conformation of the spike. Several of these monoclonal antibodies are promising candidates for clinical development as potential therapeutic and/or prophylactic agents against SARS-CoV-2. A diverse collection of potent neutralizing antibodies against the SARS-CoV-2 spike protein have been isolated from five patients with severe COVID-19 and high serum neutralization titres.

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