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Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases

Immune surveillance and adaptive immune responses, involving continuously circulating and tissue-resident T-lymphocytes, provide host defense against infectious agents and possible malignant transformation while avoiding autoimmune tissue damage. Activation, migration, and deployment of T-cells to a...

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Autores principales: Antony, Irene Rose, Wong, Brandon Han Siang, Kelleher, Dermot, Verma, Navin Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650071/
https://www.ncbi.nlm.nih.gov/pubmed/37947619
http://dx.doi.org/10.3390/cells12212541
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author Antony, Irene Rose
Wong, Brandon Han Siang
Kelleher, Dermot
Verma, Navin Kumar
author_facet Antony, Irene Rose
Wong, Brandon Han Siang
Kelleher, Dermot
Verma, Navin Kumar
author_sort Antony, Irene Rose
collection PubMed
description Immune surveillance and adaptive immune responses, involving continuously circulating and tissue-resident T-lymphocytes, provide host defense against infectious agents and possible malignant transformation while avoiding autoimmune tissue damage. Activation, migration, and deployment of T-cells to affected tissue sites are crucial for mounting an adaptive immune response. An effective adaptive immune defense depends on the ability of T-cells to dynamically reprogram their metabolic requirements in response to environmental cues. Inability of the T-cells to adapt to specific metabolic demands may skew cells to become either hyporesponsive (creating immunocompromised conditions) or hyperactive (causing autoimmune tissue destruction). Here, we review maladaptive T-cell metabolic fitness that can cause autoimmune diseases and discuss how T-cell metabolic programs can potentially be modulated to achieve therapeutic benefits.
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spelling pubmed-106500712023-10-29 Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases Antony, Irene Rose Wong, Brandon Han Siang Kelleher, Dermot Verma, Navin Kumar Cells Review Immune surveillance and adaptive immune responses, involving continuously circulating and tissue-resident T-lymphocytes, provide host defense against infectious agents and possible malignant transformation while avoiding autoimmune tissue damage. Activation, migration, and deployment of T-cells to affected tissue sites are crucial for mounting an adaptive immune response. An effective adaptive immune defense depends on the ability of T-cells to dynamically reprogram their metabolic requirements in response to environmental cues. Inability of the T-cells to adapt to specific metabolic demands may skew cells to become either hyporesponsive (creating immunocompromised conditions) or hyperactive (causing autoimmune tissue destruction). Here, we review maladaptive T-cell metabolic fitness that can cause autoimmune diseases and discuss how T-cell metabolic programs can potentially be modulated to achieve therapeutic benefits. MDPI 2023-10-29 /pmc/articles/PMC10650071/ /pubmed/37947619 http://dx.doi.org/10.3390/cells12212541 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Antony, Irene Rose
Wong, Brandon Han Siang
Kelleher, Dermot
Verma, Navin Kumar
Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title_full Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title_fullStr Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title_full_unstemmed Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title_short Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases
title_sort maladaptive t-cell metabolic fitness in autoimmune diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650071/
https://www.ncbi.nlm.nih.gov/pubmed/37947619
http://dx.doi.org/10.3390/cells12212541
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