Cargando…

T‐cell responses and therapies against SARS‐CoV‐2 infection

Coronavirus disease 2019 (COVID‐19) is caused by SARS‐CoV‐2, a novel coronavirus strain. Some studies suggest that COVID‐19 could be an immune‐related disease, and failure of effective immune responses in initial stages of viral infection could contribute to systemic inflammation and tissue damage,...

Descripción completa

Detalles Bibliográficos
Autores principales: Toor, Salman M., Saleh, Reem, Sasidharan Nair, Varun, Taha, Rowaida Z., Elkord, Eyad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730020/
https://www.ncbi.nlm.nih.gov/pubmed/32935333
http://dx.doi.org/10.1111/imm.13262
_version_ 1783621589618655232
author Toor, Salman M.
Saleh, Reem
Sasidharan Nair, Varun
Taha, Rowaida Z.
Elkord, Eyad
author_facet Toor, Salman M.
Saleh, Reem
Sasidharan Nair, Varun
Taha, Rowaida Z.
Elkord, Eyad
author_sort Toor, Salman M.
collection PubMed
description Coronavirus disease 2019 (COVID‐19) is caused by SARS‐CoV‐2, a novel coronavirus strain. Some studies suggest that COVID‐19 could be an immune‐related disease, and failure of effective immune responses in initial stages of viral infection could contribute to systemic inflammation and tissue damage, leading to worse disease outcomes. T cells can act as a double‐edge sword with both pro‐ and anti‐roles in the progression of COVID‐19. Thus, better understanding of their roles in immune responses to SARS‐CoV‐2 infection is crucial. T cells primarily react to the spike protein on the coronavirus to initiate antiviral immunity; however, T‐cell responses can be suboptimal, impaired or excessive in severe COVID‐19 patients. This review focuses on the multifaceted roles of T cells in COVID‐19 pathogenesis and rationalizes their significance in eliciting appropriate antiviral immune responses in COVID‐19 patients and unexposed individuals. In addition, we summarize the potential therapeutic approaches related to T cells to treat COVID‐19 patients. These include adoptive T‐cell therapies, vaccines activating T‐cell responses, recombinant cytokines, Th1 activators and Th17 blockers, and potential utilization of immune checkpoint inhibitors alone or in combination with anti‐inflammatory drugs to improve antiviral T‐cell responses against SARS‐CoV‐2.
format Online
Article
Text
id pubmed-7730020
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-77300202020-12-13 T‐cell responses and therapies against SARS‐CoV‐2 infection Toor, Salman M. Saleh, Reem Sasidharan Nair, Varun Taha, Rowaida Z. Elkord, Eyad Immunology Review Articles Coronavirus disease 2019 (COVID‐19) is caused by SARS‐CoV‐2, a novel coronavirus strain. Some studies suggest that COVID‐19 could be an immune‐related disease, and failure of effective immune responses in initial stages of viral infection could contribute to systemic inflammation and tissue damage, leading to worse disease outcomes. T cells can act as a double‐edge sword with both pro‐ and anti‐roles in the progression of COVID‐19. Thus, better understanding of their roles in immune responses to SARS‐CoV‐2 infection is crucial. T cells primarily react to the spike protein on the coronavirus to initiate antiviral immunity; however, T‐cell responses can be suboptimal, impaired or excessive in severe COVID‐19 patients. This review focuses on the multifaceted roles of T cells in COVID‐19 pathogenesis and rationalizes their significance in eliciting appropriate antiviral immune responses in COVID‐19 patients and unexposed individuals. In addition, we summarize the potential therapeutic approaches related to T cells to treat COVID‐19 patients. These include adoptive T‐cell therapies, vaccines activating T‐cell responses, recombinant cytokines, Th1 activators and Th17 blockers, and potential utilization of immune checkpoint inhibitors alone or in combination with anti‐inflammatory drugs to improve antiviral T‐cell responses against SARS‐CoV‐2. John Wiley and Sons Inc. 2020-10-27 2021-01 /pmc/articles/PMC7730020/ /pubmed/32935333 http://dx.doi.org/10.1111/imm.13262 Text en © 2020 The Authors. Immunology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Toor, Salman M.
Saleh, Reem
Sasidharan Nair, Varun
Taha, Rowaida Z.
Elkord, Eyad
T‐cell responses and therapies against SARS‐CoV‐2 infection
title T‐cell responses and therapies against SARS‐CoV‐2 infection
title_full T‐cell responses and therapies against SARS‐CoV‐2 infection
title_fullStr T‐cell responses and therapies against SARS‐CoV‐2 infection
title_full_unstemmed T‐cell responses and therapies against SARS‐CoV‐2 infection
title_short T‐cell responses and therapies against SARS‐CoV‐2 infection
title_sort t‐cell responses and therapies against sars‐cov‐2 infection
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730020/
https://www.ncbi.nlm.nih.gov/pubmed/32935333
http://dx.doi.org/10.1111/imm.13262
work_keys_str_mv AT toorsalmanm tcellresponsesandtherapiesagainstsarscov2infection
AT salehreem tcellresponsesandtherapiesagainstsarscov2infection
AT sasidharannairvarun tcellresponsesandtherapiesagainstsarscov2infection
AT taharowaidaz tcellresponsesandtherapiesagainstsarscov2infection
AT elkordeyad tcellresponsesandtherapiesagainstsarscov2infection