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SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19
Over the past year, numerous studies in the peer reviewed and preprint literature have reported on the virological, epidemiological and clinical characteristics of the coronavirus, SARS-CoV-2. To date, 25 studies have investigated and identified SARS-CoV-2-derived T cell epitopes in humans. Here, we...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139264/ https://www.ncbi.nlm.nih.gov/pubmed/34237248 http://dx.doi.org/10.1016/j.chom.2021.05.010 |
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author | Grifoni, Alba Sidney, John Vita, Randi Peters, Bjoern Crotty, Shane Weiskopf, Daniela Sette, Alessandro |
author_facet | Grifoni, Alba Sidney, John Vita, Randi Peters, Bjoern Crotty, Shane Weiskopf, Daniela Sette, Alessandro |
author_sort | Grifoni, Alba |
collection | PubMed |
description | Over the past year, numerous studies in the peer reviewed and preprint literature have reported on the virological, epidemiological and clinical characteristics of the coronavirus, SARS-CoV-2. To date, 25 studies have investigated and identified SARS-CoV-2-derived T cell epitopes in humans. Here, we review these recent studies, how they were performed, and their findings. We review how epitopes identified throughout the SARS-CoV2 proteome reveal significant correlation between number of epitopes defined and size of the antigen provenance. We also report additional analysis of SARS-CoV-2 human CD4 and CD8 T cell epitope data compiled from these studies, identifying 1,400 different reported SARS-CoV-2 epitopes and revealing discrete immunodominant regions of the virus and epitopes that are more prevalently recognized. This remarkable breadth of epitope repertoire has implications for vaccine design, cross-reactivity, and immune escape by SARS-CoV-2 variants. |
format | Online Article Text |
id | pubmed-8139264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81392642021-05-24 SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 Grifoni, Alba Sidney, John Vita, Randi Peters, Bjoern Crotty, Shane Weiskopf, Daniela Sette, Alessandro Cell Host Microbe Review Over the past year, numerous studies in the peer reviewed and preprint literature have reported on the virological, epidemiological and clinical characteristics of the coronavirus, SARS-CoV-2. To date, 25 studies have investigated and identified SARS-CoV-2-derived T cell epitopes in humans. Here, we review these recent studies, how they were performed, and their findings. We review how epitopes identified throughout the SARS-CoV2 proteome reveal significant correlation between number of epitopes defined and size of the antigen provenance. We also report additional analysis of SARS-CoV-2 human CD4 and CD8 T cell epitope data compiled from these studies, identifying 1,400 different reported SARS-CoV-2 epitopes and revealing discrete immunodominant regions of the virus and epitopes that are more prevalently recognized. This remarkable breadth of epitope repertoire has implications for vaccine design, cross-reactivity, and immune escape by SARS-CoV-2 variants. Elsevier Inc. 2021-07-14 2021-05-21 /pmc/articles/PMC8139264/ /pubmed/34237248 http://dx.doi.org/10.1016/j.chom.2021.05.010 Text en © 2021 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Grifoni, Alba Sidney, John Vita, Randi Peters, Bjoern Crotty, Shane Weiskopf, Daniela Sette, Alessandro SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title | SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title_full | SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title_fullStr | SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title_full_unstemmed | SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title_short | SARS-CoV-2 human T cell epitopes: Adaptive immune response against COVID-19 |
title_sort | sars-cov-2 human t cell epitopes: adaptive immune response against covid-19 |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139264/ https://www.ncbi.nlm.nih.gov/pubmed/34237248 http://dx.doi.org/10.1016/j.chom.2021.05.010 |
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