Metabolic adaptations driving innate immune memory: mechanisms and therapeutic implications.

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Dan Hao, Margaret A McBride, Julia K Bohannon, Antonio Hernandez, Benjamin Klein, David L Williams, Edward R Sherwood
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引用次数: 0

Abstract

Immune memory is a hallmark of the adaptive immune system. However, recent research reveals that innate immune cells also retain memory of prior pathogen exposure that prompts enhanced responses to subsequent infections. This phenomenon is termed "innate immune memory" or "trained immunity." Notably, remodeling of cellular metabolism, which closely links to epigenetic reprograming, is a prominent feature of innate immune memory. Adaptations in glycolysis, the tricarboxylic acid cycle, oxidative phosphorylation, glutaminolysis, and lipid synthesis pathways are critical for establishing innate immune memory. This review provides an overview of the current understanding of how metabolic adaptations drive innate immune memory. This understanding is fundamental to understanding innate immune system functions and advancing therapies against infectious diseases.

代谢适应驱动先天免疫记忆:机制和治疗意义。
免疫记忆是适应性免疫系统的标志。然而,最近的研究表明,先天免疫细胞也保留了先前病原体暴露的记忆,从而增强了对随后感染的反应。这种现象被称为“先天免疫记忆”或“训练免疫”。值得注意的是,细胞代谢的重塑与表观遗传重编程密切相关,是先天免疫记忆的一个突出特征。糖酵解、三羧酸(TCA)循环、氧化磷酸化(OXPHOS)、谷氨酰胺解和脂质合成途径的适应对于建立先天免疫记忆至关重要。这篇综述概述了目前对代谢适应如何驱动先天免疫记忆的理解。这种理解是理解先天免疫系统功能和推进针对传染病的治疗的基础。
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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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