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T cell immunity to SARS-CoV-2

Exceptional efforts have been undertaken to shed light into the biology of adaptive immune responses to SARS-CoV-2. T cells occupy a central role in adaptive immunity to mediate helper functions to different arms of the immune system and are fundamental to mediate protection, control, and clearance...

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Detalles Bibliográficos
Autores principales: Niessl, Julia, Sekine, Takuya, Buggert, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529278/
https://www.ncbi.nlm.nih.gov/pubmed/34711489
http://dx.doi.org/10.1016/j.smim.2021.101505
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author Niessl, Julia
Sekine, Takuya
Buggert, Marcus
author_facet Niessl, Julia
Sekine, Takuya
Buggert, Marcus
author_sort Niessl, Julia
collection PubMed
description Exceptional efforts have been undertaken to shed light into the biology of adaptive immune responses to SARS-CoV-2. T cells occupy a central role in adaptive immunity to mediate helper functions to different arms of the immune system and are fundamental to mediate protection, control, and clearance of most viral infections. Even though many questions remain unsolved, there is a growing literature linking specific T cell characteristics to differential COVID-19 severity and vaccine outcome. In this review, we summarize our current understanding of CD4(+) and CD8(+) T cell responses in acute and convalescent COVID-19. Further, we discuss the T cell literature coupled to pre-existing immunity and vaccines and highlight the need to look beyond blood to fully understand how T cells function in the tissue space.
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spelling pubmed-85292782021-10-21 T cell immunity to SARS-CoV-2 Niessl, Julia Sekine, Takuya Buggert, Marcus Semin Immunol Article Exceptional efforts have been undertaken to shed light into the biology of adaptive immune responses to SARS-CoV-2. T cells occupy a central role in adaptive immunity to mediate helper functions to different arms of the immune system and are fundamental to mediate protection, control, and clearance of most viral infections. Even though many questions remain unsolved, there is a growing literature linking specific T cell characteristics to differential COVID-19 severity and vaccine outcome. In this review, we summarize our current understanding of CD4(+) and CD8(+) T cell responses in acute and convalescent COVID-19. Further, we discuss the T cell literature coupled to pre-existing immunity and vaccines and highlight the need to look beyond blood to fully understand how T cells function in the tissue space. The Authors. Published by Elsevier Ltd. 2021-06 2021-10-21 /pmc/articles/PMC8529278/ /pubmed/34711489 http://dx.doi.org/10.1016/j.smim.2021.101505 Text en © 2021 The Authors 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 Article
Niessl, Julia
Sekine, Takuya
Buggert, Marcus
T cell immunity to SARS-CoV-2
title T cell immunity to SARS-CoV-2
title_full T cell immunity to SARS-CoV-2
title_fullStr T cell immunity to SARS-CoV-2
title_full_unstemmed T cell immunity to SARS-CoV-2
title_short T cell immunity to SARS-CoV-2
title_sort t cell immunity to sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529278/
https://www.ncbi.nlm.nih.gov/pubmed/34711489
http://dx.doi.org/10.1016/j.smim.2021.101505
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