嵌合抗原受体
线粒体
长寿
重编程
生物
细胞生物学
免疫学
受体
持久性(不连续性)
癌症
神经科学
线粒体融合
癌症研究
癌症治疗
线粒体生物发生
免疫疗法
线粒体DNA
信号转导
生物能学
粒线体疾病
癌症免疫疗法
生物信息学
抗原
作者
Hosein Rostamian,Mohammad Khakpoor-Koosheh,Keyvan Fallah-Mehrjardi,Hamid R. Mirzaei,Christine E. Brown
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.
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