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A combination of cross-neutralizing antibodies synergizes to prevent SARS-CoV-2 and SARS-CoV pseudovirus infection
Hejun Liu; Meng Yuan; Deli Huang; Sandhya Bangaru; Chang-Chun D. Lee; Linghang Peng; Xueyong Zhu; David Nemazee; Marit J. van Gils; Rogier W. Sanders; Hans-Christian Kornau; S. Momsen Reincke; Harald Pruss; Jakob Kreye; Nicholas C. Wu; Andrew B. Ward; Ian A. Wilson.
Affiliation
  • Hejun Liu; The Scripps Research Institute
  • Meng Yuan; The Scripps Research Institute
  • Deli Huang; The Scripps Research Institute
  • Sandhya Bangaru; The Scripps Research Institute
  • Chang-Chun D. Lee; The Scripps Research Institute
  • Linghang Peng; The Scripps Research Institute
  • Xueyong Zhu; The Scripps Research Institute
  • David Nemazee; The Scripps Research Institute
  • Marit J. van Gils; University of Amsterdam
  • Rogier W. Sanders; University of Amsterdam
  • Hans-Christian Kornau; German Center for Neurodegenerative Diseases (DZNE) Berlin
  • S. Momsen Reincke; German Center for Neurodegenerative Diseases (DZNE) Berlin
  • Harald Pruss; German Center for Neurodegenerative Diseases (DZNE) Berlin
  • Jakob Kreye; German Center for Neurodegenerative Diseases (DZNE) Berlin
  • Nicholas C. Wu; University of Illinois at Urbana-Champaign
  • Andrew B. Ward; The Scripps Research Institute
  • Ian A. Wilson; The Scripps Research Institute
Preprint in English | bioRxiv | ID: ppbiorxiv-430866
ABSTRACT
Coronaviruses have caused several epidemics and pandemics including the ongoing coronavirus disease 2019 (COVID-19). Some prophylactic vaccines and therapeutic antibodies have already showed 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. Our structural findings provide mechanistic insights into how this antibody can accommodate antigenic variation in these viruses. CV38-142 synergizes with other cross-neutralizing antibodies, in particular COVA1-16, to enhance neutralization of SARS-CoV-2 and SARS-CoV. 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 coronaviruses.
License
cc_by_nc
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Rct Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Rct Language: English Year: 2021 Document type: Preprint
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