脂质代谢
肿瘤微环境
CD8型
免疫系统
细胞毒性T细胞
生物
癌症研究
免疫检查点
效应器
细胞代谢
癌症
新陈代谢
重编程
细胞
免疫疗法
免疫学
内分泌学
生物化学
遗传学
体外
作者
Runxian Wang,Zhenya Liu,Zhiyao Fan,Hanxiang Zhan
出处
期刊:Cancer Letters
[Elsevier]
日期:2023-06-12
卷期号:567: 216267-216267
被引量:22
标识
DOI:10.1016/j.canlet.2023.216267
摘要
Effector, memory and exhaustion are three phenotypes of CD8+ T cell. In tumor microenvironment (TME), metabolism dysfunction of the three should take the blame for immune escape. Against background of CD8+ T cell in normal development, multiple determinants in TME, including nutrition competition, PD-1 signals and other cancer - CD8+ T cell interactions, cause metabolism reprograming, including failure in energy metabolism and other abnormal lipid metabolism. Further, incompatibility among metabolism patterns of three phenotypes results in unresponsiveness of immune checkpoint blockade (ICB). Therefore, combination of ICB and drugs aiming at abnormal lipid metabolism provides promising direction to improve cancer therapy. This review focuses on lipid metabolism of CD8+ T cell and aims to provide innovative therapy strategy to cure cancer.
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