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Negligible impact of SARS-CoV-2 variants on CD4+ and CD8+ T cell reactivity in COVID-19 exposed donors and vaccinees.
Alison Tarke; John Sidney; Nils Methot; Yun Zhang; Jennifer M Dan; Benjamin Goodwin; Paul Rubiro; Aaron Sutherland; Ricardo da Silva Antunes; April Fraizer; Stephen A. Rawlings; Davey M. Smith; Bjoern Peters; Richard H. Scheuermann; Daniela Weiskopf; Shane Crotty; Alba Grifoni; Alessandro Sette.
Afiliação
  • Alison Tarke; La Jolla Institute for immunology
  • John Sidney; La Jolla Institute for immunology
  • Nils Methot; La Jolla Institute for immunology
  • Yun Zhang; J. Craig Venter Institute
  • Jennifer M Dan; La Jolla Institute for Immunology
  • Benjamin Goodwin; La Jolla Institute for immunology
  • Paul Rubiro; La Jolla Institute for immunology
  • Aaron Sutherland; La Jolla Institute for immunology
  • Ricardo da Silva Antunes; La Jolla Institute for Immunology
  • April Fraizer; La Jolla Institute for immunology
  • Stephen A. Rawlings; University of California San Diego (UCSD)
  • Davey M. Smith; University of California San Diego (UCSD)
  • Bjoern Peters; La Jolla Institute for Immunology
  • Richard H. Scheuermann; J. Craig Venter Institute
  • Daniela Weiskopf; La Jolla Institute for Immunology
  • Shane Crotty; La Jolla Institute for immunology
  • Alba Grifoni; La Jolla Institute for Immunology
  • Alessandro Sette; La Jolla Institute for immunology
Preprint em En | PREPRINT-BIORXIV | ID: ppbiorxiv-433180
ABSTRACT
The emergence of SARS-CoV-2 variants highlighted the need to better understand adaptive immune responses to this virus. It is important to address whether also CD4+ and CD8+ T cell responses are affected, because of the role they play in disease resolution and modulation of COVID-19 disease severity. Here we performed a comprehensive analysis of SARS-CoV-2-specific CD4+ and CD8+ T cell responses from COVID-19 convalescent subjects recognizing the ancestral strain, compared to variant lineages B.1.1.7, B.1.351, P.1, and CAL.20C as well as recipients of the Moderna (mRNA-1273) or Pfizer/BioNTech (BNT162b2) COVID-19 vaccines. Similarly, we demonstrate that the sequences of the vast majority of SARS-CoV-2 T cell epitopes are not affected by the mutations found in the variants analyzed. Overall, the results demonstrate that CD4+ and CD8+ T cell responses in convalescent COVID-19 subjects or COVID-19 mRNA vaccinees are not substantially affected by mutations found in the SARS-CoV-2 variants.
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Tipo de estudo: Experimental_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-BIORXIV Tipo de estudo: Experimental_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint