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The impact of viral mutations on recognition by SARS-CoV-2 specific T-cells
Thushan I de Silva; Guihai Liu; Benjamin B Lindsey; Danning Dong; Dhruv Shah; Alexander J Mentzer; Adrienn Angyal; Rebecca Brown; Matthew D Parker; Zixi Yin; Xuan Yao; Lance Turtle; Susanna Dunachie; - COVID-19 Genomics UK (COG-UK) Consortium; Mala K Maini; Graham Ogg; Julian Charles Knight; Yanchun Peng; Sarah L Rowland-Jones; Tao Dong.
Afiliación
  • Thushan I de Silva; University of Sheffield
  • Guihai Liu; University of Oxford
  • Benjamin B Lindsey; University of Sheffield
  • Danning Dong; University of Oxford
  • Dhruv Shah; University of Sheffield
  • Alexander J Mentzer; University of Oxford
  • Adrienn Angyal; The University of Sheffield Medical School
  • Rebecca Brown; University of Sheffield
  • Matthew D Parker; The University of Sheffield
  • Zixi Yin; Weatherall Institute of Molecular Medicine
  • Xuan Yao; University of Oxford
  • Lance Turtle; University of Liverpool
  • Susanna Dunachie; University of Oxford
  • - COVID-19 Genomics UK (COG-UK) Consortium; -
  • Mala K Maini; University College London
  • Graham Ogg; University of Oxford
  • Julian Charles Knight; Oxford University
  • Yanchun Peng; University of Oxford
  • Sarah L Rowland-Jones; University of Sheffield
  • Tao Dong; University of Oxford
Preprint en Inglés | bioRxiv | ID: ppbiorxiv-438904
Artículo de revista
Un artículo publicado en revista científica está disponible y probablemente es basado en este preprint, por medio del reconocimiento de similitud realizado por una máquina. La confirmación humana aún está pendiente.
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ABSTRACT
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-{gamma} and cytotoxic killing assays. 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.
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Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Tipo de estudio: Experimental_studies Idioma: Inglés Año: 2021 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: bioRxiv Tipo de estudio: Experimental_studies Idioma: Inglés Año: 2021 Tipo del documento: Preprint
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