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Sensitivity of infectious SARS-CoV-2 B.1.1.7 and B.1.351 variants to neutralizing antibodies.
Planas, Delphine; Bruel, Timothée; Grzelak, Ludivine; Guivel-Benhassine, Florence; Staropoli, Isabelle; Porrot, Françoise; Planchais, Cyril; Buchrieser, Julian; Rajah, Maaran Michael; Bishop, Elodie; Albert, Mélanie; Donati, Flora; Prot, Matthieu; Behillil, Sylvie; Enouf, Vincent; Maquart, Marianne; Smati-Lafarge, Mounira; Varon, Emmanuelle; Schortgen, Frédérique; Yahyaoui, Layla; Gonzalez, Maria; De Sèze, Jérôme; Péré, Hélène; Veyer, David; Sève, Aymeric; Simon-Lorière, Etienne; Fafi-Kremer, Samira; Stefic, Karl; Mouquet, Hugo; Hocqueloux, Laurent; van der Werf, Sylvie; Prazuck, Thierry; Schwartz, Olivier.
Afiliación
  • Planas D; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Bruel T; CNRS UMR 3569, Paris, France.
  • Grzelak L; Vaccine Research Institute, Créteil, France.
  • Guivel-Benhassine F; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Staropoli I; CNRS UMR 3569, Paris, France.
  • Porrot F; Vaccine Research Institute, Créteil, France.
  • Planchais C; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Buchrieser J; CNRS UMR 3569, Paris, France.
  • Rajah MM; Vaccine Research Institute, Créteil, France.
  • Bishop E; Université de Paris, Sorbonne Paris Cité, Paris, France.
  • Albert M; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Donati F; CNRS UMR 3569, Paris, France.
  • Prot M; Vaccine Research Institute, Créteil, France.
  • Behillil S; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Enouf V; CNRS UMR 3569, Paris, France.
  • Maquart M; Vaccine Research Institute, Créteil, France.
  • Smati-Lafarge M; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Varon E; CNRS UMR 3569, Paris, France.
  • Schortgen F; Vaccine Research Institute, Créteil, France.
  • Yahyaoui L; Laboratory of Humoral Immunology, Department of Immunology, Institut Pasteur, INSERM U1222, Paris, France.
  • Gonzalez M; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • De Sèze J; CNRS UMR 3569, Paris, France.
  • Péré H; Vaccine Research Institute, Créteil, France.
  • Veyer D; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Sève A; CNRS UMR 3569, Paris, France.
  • Simon-Lorière E; Vaccine Research Institute, Créteil, France.
  • Fafi-Kremer S; Université de Paris, Sorbonne Paris Cité, Paris, France.
  • Stefic K; Virus & Immunity Unit, Department of Virology, Institut Pasteur, Paris, France.
  • Mouquet H; CNRS UMR 3569, Paris, France.
  • Hocqueloux L; Vaccine Research Institute, Créteil, France.
  • van der Werf S; Université de Paris, Sorbonne Paris Cité, Paris, France.
  • Prazuck T; Molecular Genetics of RNA Viruses, Department of Virology, Institut Pasteur CNRS UMR 3569, Université de Paris, Paris, France.
  • Schwartz O; National Reference Center for Respiratory Viruses, Institut Pasteur, Paris, France.
Nat Med ; 27(5): 917-924, 2021 05.
Article en En | MEDLINE | ID: mdl-33772244
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) B.1.1.7 and B.1.351 variants were first identified in the United Kingdom and South Africa, respectively, and have since spread to many countries. These variants harboring diverse mutations in the gene encoding the spike protein raise important concerns about their immune evasion potential. Here, we isolated infectious B.1.1.7 and B.1.351 strains from acutely infected individuals. We examined sensitivity of the two variants to SARS-CoV-2 antibodies present in sera and nasal swabs from individuals infected with previously circulating strains or who were recently vaccinated, in comparison with a D614G reference virus. We utilized a new rapid neutralization assay, based on reporter cells that become positive for GFP after overnight infection. Sera from 58 convalescent individuals collected up to 9 months after symptoms, similarly neutralized B.1.1.7 and D614G. In contrast, after 9 months, convalescent sera had a mean sixfold reduction in neutralizing titers, and 40% of the samples lacked any activity against B.1.351. Sera from 19 individuals vaccinated twice with Pfizer Cominarty, longitudinally tested up to 6 weeks after vaccination, were similarly potent against B.1.1.7 but less efficacious against B.1.351, when compared to D614G. Neutralizing titers increased after the second vaccine dose, but remained 14-fold lower against B.1.351. In contrast, sera from convalescent or vaccinated individuals similarly bound the three spike proteins in a flow cytometry-based serological assay. Neutralizing antibodies were rarely detected in nasal swabs from vaccinees. Thus, faster-spreading SARS-CoV-2 variants acquired a partial resistance to neutralizing antibodies generated by natural infection or vaccination, which was most frequently detected in individuals with low antibody levels. Our results indicate that B1.351, but not B.1.1.7, may increase the risk of infection in immunized individuals.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 2_ODS3 / 4_TD Problema de salud: 1_doencas_transmissiveis / 2_enfermedades_transmissibles / 2_muertes_prematuras_enfermedades_notrasmisibles / 4_pneumonia Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Antivirales Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 2_ODS3 / 4_TD Problema de salud: 1_doencas_transmissiveis / 2_enfermedades_transmissibles / 2_muertes_prematuras_enfermedades_notrasmisibles / 4_pneumonia Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Antivirales Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2021 Tipo del documento: Article País de afiliación: Francia
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