Your browser doesn't support javascript.
loading
The impact of Spike mutations on SARS-CoV-2 neutralization
Chloe Rees-Spear; Luke Muir; Sarah A Griffith; Judith Heaney; Yoann Aldon; Jonne Snitselaar; Peter Thomas; Carl Graham; Jeffrey Seow; Nayung Lee; Annachiara Rosa; Chloe Roustan; Catherine F Houlihan; Rogier W Sanders; Ravindra K Gupta; Peter Cherepanov; Hans Stauss; Eleni Nastouli; Katie J Doores; Marit J van Gils; Laura E McCoy.
Afiliación
  • Chloe Rees-Spear; University College London
  • Luke Muir; University College London
  • Sarah A Griffith; University College London
  • Judith Heaney; University College London Hospitals
  • Yoann Aldon; Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam Institute for Infection and Immunity, Netherlands
  • Jonne Snitselaar; Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam Institute for Infection and Immunity, Netherlands
  • Peter Thomas; University College London
  • Carl Graham; Kings College London
  • Jeffrey Seow; Kings College London
  • Nayung Lee; University College London
  • Annachiara Rosa; The Francis Crick Institute, UK
  • Chloe Roustan; The Francis Crick Institute, UK
  • Catherine F Houlihan; University College London
  • Rogier W Sanders; Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Amsterdam Institute for Infection and Immunity, Netherlands
  • Ravindra K Gupta; University of Cambridge
  • Peter Cherepanov; The Francis Crick Institute
  • Hans Stauss; University College London
  • Eleni Nastouli; University College London
  • Katie J Doores; Kings College London
  • Marit J van Gils; Academic Medical Center Amsterdam
  • Laura E McCoy; University College London
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-426849
ABSTRACT
Multiple SARS-CoV-2 vaccines have shown protective efficacy, which is most likely mediated by neutralizing antibodies recognizing the viral entry protein, Spike. Antibodies from SARS-CoV-2 infection neutralize the virus by focused targeting of Spike and there is limited serum cross-neutralization of the closely-related SARS-CoV. As new SARS-CoV-2 variants are rapidly emerging, exemplified by the B.1.1.7, 501Y.V2 and P.1 lineages, it is critical to understand if antibody responses induced by infection with the original SARS-CoV-2 virus or the current vaccines will remain effective against virus variants. In this study we evaluate neutralization of a series of mutated Spike pseudotypes including a B.1.1.7 Spike pseudotype. The analyses of a panel of Spike-specific monoclonal antibodies revealed that the neutralizing activity of some antibodies was dramatically reduced by Spike mutations. In contrast, polyclonal antibodies in the serum of patients infected in early 2020 remained active against most mutated Spike pseudotypes. The majority of serum samples were equally able to neutralize the B.1.1.7 Spike pseudotype, however potency was reduced in a small number of samples (3 of 36) by 5-10-fold. This work highlights that changes in the SARS-CoV-2 Spike can alter neutralization sensitivity and underlines the need for effective real-time monitoring of emerging mutations and their impact on vaccine efficacy.
Licencia
cc_by_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Experimental_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Experimental_studies / Rct Idioma: En Año: 2021 Tipo del documento: Preprint