Age- and diet-instructed metabolic rewiring of the tumor-immune microenvironment.

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-06-02 Epub Date: 2025-04-11 DOI:10.1084/jem.20241102
Ana Belén Plata-Gómez, Ping-Chih Ho
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引用次数: 0

Abstract

The tumor-immune microenvironment (TIME) plays a critical role in tumor development and metastasis, as it influences the evolution of tumor cells and fosters an immunosuppressive state by intervening the metabolic reprogramming of infiltrating immune cells. Aging and diet significantly impact the metabolic reprogramming of the TIME, contributing to cancer progression and immune evasion. With aging, immune cell function declines, leading to a proinflammatory state and metabolic alterations such as increased oxidative stress and mitochondrial dysfunction, which compromise antitumor immunity. Similarly, dietary factors, particularly high-fat and high-sugar diets, promote metabolic shifts, creating a permissive TIME by fostering tumor-supportive immune cell phenotypes while impairing the tumoricidal activity of immune cells. In contrast, dietary restrictions have been shown to restore immune function by modulating metabolism and enhancing antitumor immune responses. Here, we discuss the intricate interplay between aging, diet, and metabolic reprogramming in shaping the TIME, with a particular focus on T cells, and highlight therapeutic strategies targeting these pathways to empower antitumor immunity.

年龄和饮食指示的肿瘤免疫微环境的代谢重新布线。
肿瘤免疫微环境(tumor-immune microenvironment, TIME)通过干预浸润性免疫细胞的代谢重编程,影响肿瘤细胞的进化,形成免疫抑制状态,在肿瘤的发生和转移过程中起着至关重要的作用。衰老和饮食显著影响时间的代谢重编程,促进癌症进展和免疫逃避。随着年龄的增长,免疫细胞功能下降,导致促炎状态和代谢改变,如氧化应激增加和线粒体功能障碍,从而损害抗肿瘤免疫。同样,饮食因素,特别是高脂肪和高糖饮食,促进代谢变化,通过培养肿瘤支持免疫细胞表型,同时损害免疫细胞的杀肿瘤活性,创造一个允许的时间。相反,饮食限制已被证明通过调节代谢和增强抗肿瘤免疫反应来恢复免疫功能。在这里,我们讨论了衰老、饮食和代谢重编程在形成时间中的复杂相互作用,特别关注T细胞,并强调针对这些途径的治疗策略,以增强抗肿瘤免疫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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