肿瘤微环境
免疫系统
间质细胞
重编程
癌症免疫疗法
免疫疗法
生物
表观遗传学
癌症研究
癌细胞
癌症
细胞毒性T细胞
巨噬细胞
细胞生物学
免疫学
细胞
体外
生物化学
基因
遗传学
作者
Stefania Vilbois,Yingxi Xu,Ping‐Chih Ho
标识
DOI:10.1016/j.trecan.2023.11.007
摘要
The tumor microenvironment (TME) contains a complex cellular ecosystem where cancer, stromal, vascular, and immune cells interact. Macrophages and regulatory T cells (Tregs) are critical not only for maintaining immunological homeostasis and tumor growth but also for monitoring the functional states of other immune cells. Emerging evidence reveals that metabolic changes in macrophages and Tregs significantly influence their pro-/antitumor functions through the regulation of signaling cascades and epigenetic reprogramming. Hence, they are increasingly recognized as therapeutic targets in cancer immunotherapy. Specific metabolites in the TME may also affect their pro-/antitumor functions by intervening with the metabolic machinery. We discuss how metabolites influence the immunosuppressive phenotypes of tumor-associated macrophages (TAMs) and Tregs. We then describe how TAMs and Tregs, independently or collaboratively, utilize metabolic mechanisms to suppress the activity of CD8+ T cells. Finally, we highlight promising metabolic interventions that can improve the outcome of current cancer therapies.
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