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T Cell Metabolism in Infection

T lymphocytes (T cells) are divided into two functionally different subgroups the CD4+ T helper cells (Th) and the CD8+ cytotoxic T lymphocytes (CTL). Adequate CD4 and CD8 T cell activation to proliferation, clonal expansion and effector function is crucial for efficient clearance of infection by pa...

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Detalles Bibliográficos
Autores principales: Wik, Jonas Aakre, Skålhegg, Bjørn Steen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964062/
https://www.ncbi.nlm.nih.gov/pubmed/35359994
http://dx.doi.org/10.3389/fimmu.2022.840610
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author Wik, Jonas Aakre
Skålhegg, Bjørn Steen
author_facet Wik, Jonas Aakre
Skålhegg, Bjørn Steen
author_sort Wik, Jonas Aakre
collection PubMed
description T lymphocytes (T cells) are divided into two functionally different subgroups the CD4+ T helper cells (Th) and the CD8+ cytotoxic T lymphocytes (CTL). Adequate CD4 and CD8 T cell activation to proliferation, clonal expansion and effector function is crucial for efficient clearance of infection by pathogens. Failure to do so may lead to T cell exhaustion. Upon activation by antigen presenting cells, T cells undergo metabolic reprograming that support effector functions. In this review we will discuss how metabolic reprograming dictates functionality during viral infections using severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and human immunodeficiency virus (HIV) as examples. Moreover, we will briefly discuss T cell metabolic programs during bacterial infections exemplified by Mycobacterium tuberculosis (MT) infection.
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spelling pubmed-89640622022-03-30 T Cell Metabolism in Infection Wik, Jonas Aakre Skålhegg, Bjørn Steen Front Immunol Immunology T lymphocytes (T cells) are divided into two functionally different subgroups the CD4+ T helper cells (Th) and the CD8+ cytotoxic T lymphocytes (CTL). Adequate CD4 and CD8 T cell activation to proliferation, clonal expansion and effector function is crucial for efficient clearance of infection by pathogens. Failure to do so may lead to T cell exhaustion. Upon activation by antigen presenting cells, T cells undergo metabolic reprograming that support effector functions. In this review we will discuss how metabolic reprograming dictates functionality during viral infections using severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and human immunodeficiency virus (HIV) as examples. Moreover, we will briefly discuss T cell metabolic programs during bacterial infections exemplified by Mycobacterium tuberculosis (MT) infection. Frontiers Media S.A. 2022-03-14 /pmc/articles/PMC8964062/ /pubmed/35359994 http://dx.doi.org/10.3389/fimmu.2022.840610 Text en Copyright © 2022 Wik and Skålhegg https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wik, Jonas Aakre
Skålhegg, Bjørn Steen
T Cell Metabolism in Infection
title T Cell Metabolism in Infection
title_full T Cell Metabolism in Infection
title_fullStr T Cell Metabolism in Infection
title_full_unstemmed T Cell Metabolism in Infection
title_short T Cell Metabolism in Infection
title_sort t cell metabolism in infection
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964062/
https://www.ncbi.nlm.nih.gov/pubmed/35359994
http://dx.doi.org/10.3389/fimmu.2022.840610
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