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肿瘤诱导的代谢性免疫抑制:机制与治疗靶点

英文原题:Tumor-induced metabolic immunosuppression: Mechanisms and therapeutic targets.

查看英文原题

Tumor-induced metabolic immunosuppression: Mechanisms and therapeutic targets.

PubMed 2025/01/10(内容时间) Cell Rep Q1 · IF 7.7(JCR 2025)

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中文摘要

免疫细胞和癌细胞中的代谢重编程在抗肿瘤免疫应答中发挥着关键作用。近期研究表明,癌症代谢不仅通过改变信号传导维持致癌作用和生存,还调节免疫细胞功能。肿瘤微环境中的代谢串扰导致营养竞争和酸中毒,从而阻碍免疫细胞功能。有趣的是,免疫细胞也经历代谢重编程,使其能够增殖、分化和执行效应功能。本综述重点阐述了通过癌细胞和免疫细胞中的代谢重编程对抗肿瘤免疫应答的调控,并探讨了在癌症免疫治疗中靶向这些代谢途径的治疗策略,包括使用嵌合抗原受体(CAR)-T细胞。我们讨论了免疫治疗、细胞疗法和代谢干预的创新组合,这些组合可能优化现有治疗方案的效果。

展开英文摘要原文

Metabolic reprogramming in both immune and cancer cells plays a crucial role in the antitumor immune response. Recent studies indicate that cancer metabolism not only sustains carcinogenesis and survival via altered signaling but also modulates immune cell function. Metabolic crosstalk within the tumor microenvironment results in nutrient competition and acidosis, thereby hindering immune cell functionality.

Interestingly, immune cells also undergo metabolic reprogramming that enables their proliferation, differentiation, and effector functions. This review highlights the regulation of antitumor immune responses through metabolic reprogramming in cancer and immune cells and explores therapeutic strategies that target these metabolic pathways in cancer immunotherapy, including using chimeric antigen receptor (CAR)-T cells.

We discuss innovative combinations of immunotherapy, cellular therapies, and metabolic interventions that could optimize the efficacy of existing treatment protocols.

论文信息

作者
Ricci JE
单位
Université Côte d'Azur, INSERM, C3M, Nice, France; Équipe labellisée LIGUE Contre le Cancer, Nice, France. Electronic address: ricci@unice.fr.France
文献类型
综述 · 非美国政府资助研究
期刊
Cell reports2025 Jan 28
原文标识
PubMed 39798090 · DOI 10.1016/j.celrep.2024.115206