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Population immunity predicts evolutionary trajectories of SARS-CoV-2.
Meijers, Matthijs; Ruchnewitz, Denis; Eberhardt, Jan; Luksza, Marta; Lässig, Michael.
Afiliación
  • Meijers M; Institute for Biological Physics, University of Cologne, Zülpicherstr. 77, 50937 Köln, Germany.
  • Ruchnewitz D; Institute for Biological Physics, University of Cologne, Zülpicherstr. 77, 50937 Köln, Germany.
  • Eberhardt J; Institute for Biological Physics, University of Cologne, Zülpicherstr. 77, 50937 Köln, Germany.
  • Luksza M; Tisch Cancer Institute, Departments of Oncological Sciences and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Lässig M; Institute for Biological Physics, University of Cologne, Zülpicherstr. 77, 50937 Köln, Germany. Electronic address: mlaessig@uni-koeln.de.
Cell ; 186(23): 5151-5164.e13, 2023 11 09.
Article en En | MEDLINE | ID: mdl-37875109
The large-scale evolution of the SARS-CoV-2 virus has been marked by rapid turnover of genetic clades. New variants show intrinsic changes, notably increased transmissibility, and antigenic changes that reduce cross-immunity induced by previous infections or vaccinations. How this functional variation shapes global evolution has remained unclear. Here, we establish a predictive fitness model for SARS-CoV-2 that integrates antigenic and intrinsic selection. The model is informed by tracking of time-resolved sequence data, epidemiological records, and cross-neutralization data of viral variants. Our inference shows that immune pressure, including contributions of vaccinations and previous infections, has become the dominant force driving the recent evolution of SARS-CoV-2. The fitness model can serve continued surveillance in two ways. First, it successfully predicts the short-term evolution of circulating strains and flags emerging variants likely to displace the previously predominant variant. Second, it predicts likely antigenic profiles of successful escape variants prior to their emergence.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: SARS-CoV-2 / COVID-19 Límite: Humans Idioma: En Revista: Cell Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: SARS-CoV-2 / COVID-19 Límite: Humans Idioma: En Revista: Cell Año: 2023 Tipo del documento: Article País de afiliación: Alemania