Mitochondria as Playmakers of CAR T-cell Fate and Longevity.
细胞凋亡
程序性细胞死亡
细胞
T细胞
免疫系统
作者
Hosein Rostamian,Mohammad Khakpoor-Koosheh,Keyvan Fallah-Mehrjardi,Hamid Reza Mirzaei,Christine E. Brown
出处
期刊:Cancer immunology research [American Association for Cancer Research] 日期:2021-08-01卷期号:9 (8): 856-861
标识
DOI:10.1158/2326-6066.cir-21-0110
摘要
The development of chimeric antigen receptor (CAR) T-cell therapy has led to a paradigm shift in cancer treatment. However, patients often do not benefit from CAR T-cell therapy due to poor persistence of the adoptively transferred cells. Development of strategies based on the generation and maintenance of long-lasting memory T cells may expand the therapeutic effects of CAR T cells. Mitochondrial metabolic pathways play crucial roles in regulating the fate, function, and longevity of T cells. Here, we discuss how reprogramming of mitochondrial metabolic pathways influences function, persistence, and determination of CAR T-cell fate toward a memory phenotype. Moreover, we explore how mitochondrial activity determines persistence and the clinical outcome of CAR T-cell therapy. In addition, we review some strategies for manipulating CAR T-cell mitochondria to improve the survival of CAR T cells.