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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...

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Autores principales: Grifoni, Alba, Sidney, John, Vita, Randi, Peters, Bjoern, Crotty, Shane, Weiskopf, Daniela, Sette, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
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.
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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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