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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.
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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941626/ https://www.ncbi.nlm.nih.gov/pubmed/33688655 http://dx.doi.org/10.1101/2021.02.27.433180 |
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author | Tarke, Alison Sidney, John Methot, Nils Zhang, Yun Dan, Jennifer M. Goodwin, Benjamin Rubiro, Paul Sutherland, Aaron da Silva Antunes, Ricardo Frazier, April Rawlings, Stephen A. Smith, Davey M. Peters, Bjoern Scheuermann, Richard H. Weiskopf, Daniela Crotty, Shane Grifoni, Alba Sette, Alessandro |
author_facet | Tarke, Alison Sidney, John Methot, Nils Zhang, Yun Dan, Jennifer M. Goodwin, Benjamin Rubiro, Paul Sutherland, Aaron da Silva Antunes, Ricardo Frazier, April Rawlings, Stephen A. Smith, Davey M. Peters, Bjoern Scheuermann, Richard H. Weiskopf, Daniela Crotty, Shane Grifoni, Alba Sette, Alessandro |
author_sort | Tarke, Alison |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7941626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-79416262021-03-10 Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. Tarke, Alison Sidney, John Methot, Nils Zhang, Yun Dan, Jennifer M. Goodwin, Benjamin Rubiro, Paul Sutherland, Aaron da Silva Antunes, Ricardo Frazier, April Rawlings, Stephen A. Smith, Davey M. Peters, Bjoern Scheuermann, Richard H. Weiskopf, Daniela Crotty, Shane Grifoni, Alba Sette, Alessandro bioRxiv Article 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. Cold Spring Harbor Laboratory 2021-03-01 /pmc/articles/PMC7941626/ /pubmed/33688655 http://dx.doi.org/10.1101/2021.02.27.433180 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Tarke, Alison Sidney, John Methot, Nils Zhang, Yun Dan, Jennifer M. Goodwin, Benjamin Rubiro, Paul Sutherland, Aaron da Silva Antunes, Ricardo Frazier, April Rawlings, Stephen A. Smith, Davey M. Peters, Bjoern Scheuermann, Richard H. Weiskopf, Daniela Crotty, Shane Grifoni, Alba Sette, Alessandro Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title | Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title_full | Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title_fullStr | Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title_full_unstemmed | Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title_short | Negligible impact of SARS-CoV-2 variants on CD4(+) and CD8(+) T cell reactivity in COVID-19 exposed donors and vaccinees. |
title_sort | negligible impact of sars-cov-2 variants on cd4(+) and cd8(+) t cell reactivity in covid-19 exposed donors and vaccinees. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941626/ https://www.ncbi.nlm.nih.gov/pubmed/33688655 http://dx.doi.org/10.1101/2021.02.27.433180 |
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