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Sensitivity of infectious SARS-CoV-2 B.1.1.7 and B.1.351 variants to neutralizing antibodies
Delphine Planas; Timothee Bruel; Ludivine Grzelak; Florence Guivel-Benhassine; Isabelle Staropoli; Francoise Porrot; Cyril Planchais; Julian Buchrieser; Maaran Michael Rajah; Elodie Bishop; Melanie Albert; Flora Donati; Sylvie Behillil; Vincent Enouf; Maquart Marianne; Maria Gonzalez; Jerome De Seze; Helene Pere; David Veyer; Etienne Simon-Loriere; Samira Fafi-Kremer; Karl Stefic; Hugo Mouquet; Sylvie van der Werf; Olivier Schwartz.
Afiliación
  • Delphine Planas; Institut Pasteur
  • Timothee Bruel; Institut Pasteur
  • Ludivine Grzelak; Institut Pasteur
  • Florence Guivel-Benhassine; Institut Pasteur
  • Isabelle Staropoli; Institut Pasteur
  • Francoise Porrot; Institut Pasteur
  • Cyril Planchais; Institut Pasteur
  • Julian Buchrieser; Institut Pasteur
  • Maaran Michael Rajah; Institut Pasteur
  • Elodie Bishop; Institut Pasteur
  • Melanie Albert; Institut Pasteur
  • Flora Donati; INSERM U955
  • Sylvie Behillil; Institut Pasteur
  • Vincent Enouf; Insitut Pasteur
  • Maquart Marianne; Universite de Tours
  • Maria Gonzalez; Hopitaux Universitaire de Strasbourg
  • Jerome De Seze; Hopitaux Universitaires de Strasbourg
  • Helene Pere; AP-HP
  • David Veyer; AP-HP
  • Etienne Simon-Loriere; Institut Pasteur
  • Samira Fafi-Kremer; Hopitaux Universitaires de Strasbourg
  • Karl Stefic; Hopital de Tours
  • Hugo Mouquet; Institut Pasteur
  • Sylvie van der Werf; Institut Pasteur
  • Olivier Schwartz; Institut Pasteur
Preprint en Inglés | bioRxiv | ID: ppbiorxiv-430472
ABSTRACT
SARS-CoV-2 B.1.1.7 and B.1.351 variants emerged respectively in United Kingdom and South Africa and spread in many countries. Here, we isolated infectious B.1.1.7 and B.1.351 strains and examined their sensitivity to anti-SARS-CoV-2 antibodies present in sera and nasal swabs, in comparison with a D614G reference virus. We established a novel rapid neutralization assay, based on reporter cells that become GFP+ after overnight infection. B.1.1.7 was neutralized by 79/83 sera from convalescent patients collected up to 9 months post symptoms, almost similar to D614G. There was a mean 6-fold reduction in titers and even loss of activity against B.1.351 in 40% of convalescent sera after 9 months. Early sera from 19 vaccinated individuals were almost as potent against B.1.1.7 but less efficacious against B.1.351, when compared to D614G. Nasal swabs from vaccine recipients were not neutralizing, except in individuals who were diagnosed COVID-19+ before vaccination. Thus, faster-spreading variants acquired a partial resistance to humoral immunity generated by natural infection or vaccination, mostly visible in individuals with low antibody levels.
Licencia
cc_by_nc_nd
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2021 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Idioma: Inglés Año: 2021 Tipo del documento: Preprint
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