Metabolic plasticity of T cell fate decision

Abstract. The efficacy of adaptive immune responses in cancer treatment relies heavily on the state of the T cells. Upon antigen exposure, T cells undergo metabolic reprogramming, leading to the development of functional effectors or memory populations. However, within the tumor microenvironment (TM...

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Main Authors: Xiaoli Pan, Jiajia Wang, Lianjun Zhang, Guideng Li, Bo Huang, Jing Ni, Xuehong Zhang
Format: Article
Language:English
Published: Wolters Kluwer 2024-04-01
Series:Chinese Medical Journal
Online Access:http://journals.lww.com/10.1097/CM9.0000000000002989
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author Xiaoli Pan
Jiajia Wang
Lianjun Zhang
Guideng Li
Bo Huang
Jing Ni
Xuehong Zhang
author_facet Xiaoli Pan
Jiajia Wang
Lianjun Zhang
Guideng Li
Bo Huang
Jing Ni
Xuehong Zhang
author_sort Xiaoli Pan
collection DOAJ
description Abstract. The efficacy of adaptive immune responses in cancer treatment relies heavily on the state of the T cells. Upon antigen exposure, T cells undergo metabolic reprogramming, leading to the development of functional effectors or memory populations. However, within the tumor microenvironment (TME), metabolic stress impairs CD8+ T cell anti-tumor immunity, resulting in exhausted differentiation. Recent studies suggested that targeting T cell metabolism could offer promising therapeutic opportunities to enhance T cell immunotherapy. In this review, we provide a comprehensive summary of the intrinsic and extrinsic factors necessary for metabolic reprogramming during the development of effector and memory T cells in response to acute and chronic inflammatory conditions. Furthermore, we delved into the different metabolic switches that occur during T cell exhaustion, exploring how prolonged metabolic stress within the TME triggers alterations in cellular metabolism and the epigenetic landscape that contribute to T cell exhaustion, ultimately leading to a persistently exhausted state. Understanding the intricate relationship between T cell metabolism and cancer immunotherapy can lead to the development of novel approaches to improve the efficacy of T cell-based treatments against cancer.
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spelling doaj.art-c32cfccebde44a73bb0cf75c1f108b6d2024-04-04T03:29:11ZengWolters KluwerChinese Medical Journal0366-69992542-56412024-04-01137776277510.1097/CM9.0000000000002989202404050-00002Metabolic plasticity of T cell fate decisionXiaoli Pan0Jiajia Wang1Lianjun Zhang2Guideng Li3Bo Huang4Jing NiXuehong Zhang1 National Key Laboratory of Immunity and Inflammation, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Suzhou, Jiangsu 215123, China1 National Key Laboratory of Immunity and Inflammation, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Suzhou, Jiangsu 215123, China1 National Key Laboratory of Immunity and Inflammation, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Suzhou, Jiangsu 215123, China1 National Key Laboratory of Immunity and Inflammation, Suzhou Institute of Systems Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Suzhou, Jiangsu 215123, China3 Department of Immunology & National Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College, Beijing 100005, ChinaAbstract. The efficacy of adaptive immune responses in cancer treatment relies heavily on the state of the T cells. Upon antigen exposure, T cells undergo metabolic reprogramming, leading to the development of functional effectors or memory populations. However, within the tumor microenvironment (TME), metabolic stress impairs CD8+ T cell anti-tumor immunity, resulting in exhausted differentiation. Recent studies suggested that targeting T cell metabolism could offer promising therapeutic opportunities to enhance T cell immunotherapy. In this review, we provide a comprehensive summary of the intrinsic and extrinsic factors necessary for metabolic reprogramming during the development of effector and memory T cells in response to acute and chronic inflammatory conditions. Furthermore, we delved into the different metabolic switches that occur during T cell exhaustion, exploring how prolonged metabolic stress within the TME triggers alterations in cellular metabolism and the epigenetic landscape that contribute to T cell exhaustion, ultimately leading to a persistently exhausted state. Understanding the intricate relationship between T cell metabolism and cancer immunotherapy can lead to the development of novel approaches to improve the efficacy of T cell-based treatments against cancer.http://journals.lww.com/10.1097/CM9.0000000000002989
spellingShingle Xiaoli Pan
Jiajia Wang
Lianjun Zhang
Guideng Li
Bo Huang
Jing Ni
Xuehong Zhang
Metabolic plasticity of T cell fate decision
Chinese Medical Journal
title Metabolic plasticity of T cell fate decision
title_full Metabolic plasticity of T cell fate decision
title_fullStr Metabolic plasticity of T cell fate decision
title_full_unstemmed Metabolic plasticity of T cell fate decision
title_short Metabolic plasticity of T cell fate decision
title_sort metabolic plasticity of t cell fate decision
url http://journals.lww.com/10.1097/CM9.0000000000002989
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AT bohuang metabolicplasticityoftcellfatedecision
AT jingni metabolicplasticityoftcellfatedecision
AT xuehongzhang metabolicplasticityoftcellfatedecision