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A monoclonal antibody that neutralizes SARS-CoV-2 variants, SARS-CoV, and other sarbecoviruses
Pengfei Wang; Ryan G Casner; Manoj S Nair; Jian Yu; Yicheng Guo; Maple Wang; Jasper F.W. Chan; Gabriele Cerutti; Sho Iketani; Lihong Liu; Zizhang Sheng; Zhiwei Chen; Kwok-Yung Yuen; Peter D Kwong; Yaoxing Huang; Lawrence Shapiro; David D Ho.
Afiliação
  • Pengfei Wang; Fudan University
  • Ryan G Casner; Department of Biochemistry and Molecular Biophysics, Columbia University
  • Manoj S Nair; Columbia University
  • Jian Yu; Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons
  • Yicheng Guo; Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons
  • Maple Wang; Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons
  • Jasper F.W. Chan; University of Hong Kong
  • Gabriele Cerutti; Columbia University
  • Sho Iketani; Columbia University Irving Medical Center
  • Lihong Liu; Columbia University Irving Medical Center
  • Zizhang Sheng; Columbia University
  • Zhiwei Chen; The University of Hong Kong
  • Kwok-Yung Yuen; The University of Hong Kong
  • Peter D Kwong; National Institutes of Health
  • Yaoxing Huang; Columbia University
  • Lawrence Shapiro; Columbia University
  • David D Ho; Columbia University Irving Medical Center
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-464307
Artigo de periódico
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ABSTRACT
The repeated emergence of highly pathogenic human coronaviruses as well as their evolving variants highlight the need to develop potent and broad-spectrum antiviral therapeutics and vaccines. By screening monoclonal antibodies (mAbs) isolated from COVID-19-convalescent patients, we found one mAb, 2-36, with cross-neutralizing activity against SARS-CoV. We solved the cryo-EM structure of 2-36 in complex with SARS-CoV-2 or SARS-CoV spike, revealing a highly conserved epitope in the receptor-binding domain (RBD). Antibody 2-36 neutralized not only all current circulating SARS-CoV-2 variants and SARS-COV, but also a panel of bat and pangolin sarbecoviruses that can use human angiotensin-converting enzyme 2 (ACE2) as a receptor. We selected 2-36-escape viruses in vitro and confirmed that K378T in SARS-CoV-2 RBD led to viral resistance. Taken together, 2-36 represents a strategic reserve drug candidate for the prevention and treatment of possible diseases caused by pre-emergent SARS-related coronaviruses. Its epitope defines a promising target for the development of a pan-sarbecovirus vaccine.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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