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免疫代谢:信号通路、稳态及治疗靶点

Immunometabolism: signaling pathways, homeostasis, and therapeutic targets.

作者信息

Xu Rongrong, He Xiaobo, Xu Jia, Yu Ganjun, Wu Yanfeng

机构信息

National Key Laboratory of Immunity and Inflammation & Institute of Immunology College of Basic Medical Sciences Naval Medical University Shanghai China.

School of Life Sciences Fudan University Shanghai China.

出版信息

MedComm (2020). 2024 Nov 3;5(11):e789. doi: 10.1002/mco2.789. eCollection 2024 Nov.


DOI:10.1002/mco2.789
PMID:39492834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11531657/
Abstract

Immunometabolism plays a central role in sustaining immune system functionality and preserving physiological homeostasis within the organism. During the differentiation and activation, immune cells undergo metabolic reprogramming mediated by complex signaling pathways. Immune cells maintain homeostasis and are influenced by metabolic microenvironmental cues. A series of immunometabolic enzymes modulate immune cell function by metabolizing nutrients and accumulating metabolic products. These enzymes reverse immune cells' differentiation, disrupt intracellular signaling pathways, and regulate immune responses, thereby influencing disease progression. The huge population of immune metabolic enzymes, the ubiquity, and the complexity of metabolic regulation have kept the immune metabolic mechanisms related to many diseases from being discovered, and what has been revealed so far is only the tip of the iceberg. This review comprehensively summarized the immune metabolic enzymes' role in multiple immune cells such as T cells, macrophages, natural killer cells, and dendritic cells. By classifying and dissecting the immunometabolism mechanisms and the implications in diseases, summarizing and analyzing advancements in research and clinical applications of the inhibitors targeting these enzymes, this review is intended to provide a new perspective concerning immune metabolic enzymes for understanding the immune system, and offer novel insight into future therapeutic interventions.

摘要

免疫代谢在维持免疫系统功能和保持机体内生理稳态方面发挥着核心作用。在分化和激活过程中,免疫细胞会经历由复杂信号通路介导的代谢重编程。免疫细胞维持体内稳态,并受代谢微环境信号的影响。一系列免疫代谢酶通过代谢营养物质和积累代谢产物来调节免疫细胞功能。这些酶会逆转免疫细胞的分化、破坏细胞内信号通路并调节免疫反应,从而影响疾病进展。免疫代谢酶数量众多、分布广泛且代谢调节复杂,这使得与许多疾病相关的免疫代谢机制尚未被发现,目前所揭示的只是冰山一角。本综述全面总结了免疫代谢酶在T细胞、巨噬细胞、自然杀伤细胞和树突状细胞等多种免疫细胞中的作用。通过对免疫代谢机制及其在疾病中的意义进行分类和剖析,总结和分析针对这些酶的抑制剂在研究和临床应用方面的进展,本综述旨在为理解免疫系统提供有关免疫代谢酶的新视角,并为未来的治疗干预提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/af6690160c2f/MCO2-5-e789-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/8fba3ee76b36/MCO2-5-e789-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/69a1f72798b3/MCO2-5-e789-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/ae5014fa34a0/MCO2-5-e789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/af6690160c2f/MCO2-5-e789-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/8fba3ee76b36/MCO2-5-e789-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/69a1f72798b3/MCO2-5-e789-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/ae5014fa34a0/MCO2-5-e789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a9/11531657/af6690160c2f/MCO2-5-e789-g005.jpg

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Immunometabolism: signaling pathways, homeostasis, and therapeutic targets.

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引用本文的文献

[1]
Probiotic intervention alters immune gene expression and tumor characteristics in experimental breast cancer.

Mol Biol Rep. 2025-8-8

[2]
Immune inflammation and metabolic interactions in the pathogenesis of diabetic nephropathy.

Front Endocrinol (Lausanne). 2025-7-8

[3]
Discovery of CMNPD31124 as a novel marine-derived PKMYT1 inhibitor for pancreatic ductal adenocarcinoma therapy: computational and biological insights.

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[4]
Restoring immune tolerance in pre-RA: immunometabolic dialogue between gut microbiota and regulatory T cells.

Front Immunol. 2025-3-20

[5]
Molecular Mechanisms of Immune Regulation: A Review.

Cells. 2025-2-14

本文引用的文献

[1]
T cell dysfunction and therapeutic intervention in cancer.

Nat Immunol. 2024-8

[2]
MHC heterozygosity limits T cell receptor variability in CD4 T cells.

Sci Immunol. 2024-7-12

[3]
Lipid metabolism: a central modulator of RORγt-mediated Th17 cell differentiation.

Int Immunol. 2024-9-10

[4]
Arginase inhibitor reduces fungal dissemination in murine pulmonary cryptococcosis by promoting anti-cryptococcal immunity.

Int Immunopharmacol. 2024-5-10

[5]
Cellular metabolism regulates the differentiation and function of T-cell subsets.

Cell Mol Immunol. 2024-5

[6]
Pharmacological blockade of HDAC6 attenuates cancer progression by inhibiting IL-1β and modulating immunosuppressive response in OSCC.

Int Immunopharmacol. 2024-5-10

[7]
The NADase CD38 is a central regulator in gouty inflammation and a novel druggable therapeutic target.

Inflamm Res. 2024-5

[8]
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Tuberculosis (Edinb). 2024-5

[9]
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Trends Endocrinol Metab. 2024-7

[10]
Ex Vivo Efficacy of SAR442257 Anti-CD38 Trispecific T-cell Engager in Multiple Myeloma Relapsed After Daratumumab and BCMA-targeted Therapies.

Cancer Res Commun. 2024-3-12

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