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The impact of viral mutations on recognition by SARS-CoV-2 specific T cells

  • COVID-19 Genomics UK (COG-UK) Consortium
  • , ISARIC4C Investigators
  • https://www.cogconsortium.uk
  • https://isaric4c.net
  • University of Sheffield
  • London School of Hygiene & Tropical Medicine
  • University of Oxford
  • University of Oxford Medical Sciences Division
  • Capital Medical University
  • Xinjiang Medical University
  • University of Liverpool
  • Nuffield Department of Medicine
  • University of Oxford
  • Liverpool University Hospitals NHS Foundation Trust
  • Mahidol-Oxford Tropical Medicine Research Unit
  • University College London

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

76 Citas (Scopus)

Resumen

We identify amino acid variants within dominant SARS-CoV-2 T cell epitopes by interrogating global sequence data. Several variants within nucleocapsid and ORF3a epitopes have arisen independently in multiple lineages and result in loss of recognition by epitope-specific T cells assessed by IFN-γ and cytotoxic killing assays. Complete loss of T cell responsiveness was seen due to Q213K in the A∗01:01-restricted CD8+ ORF3a epitope FTSDYYQLY207-215; due to P13L, P13S, and P13T in the B∗27:05-restricted CD8+ nucleocapsid epitope QRNAPRITF9-17; and due to T362I and P365S in the A∗03:01/A∗11:01-restricted CD8+ nucleocapsid epitope KTFPPTEPK361-369. CD8+ T cell lines unable to recognize variant epitopes have diverse T cell receptor repertoires. These data demonstrate the potential for T cell evasion and highlight the need for ongoing surveillance for variants capable of escaping T cell as well as humoral immunity.

Idioma originalInglés
Número de artículo103353
PublicacióniScience
Volumen24
N.º11
DOI
EstadoPublicada - 19 nov. 2021
Publicado de forma externa

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