Boussiotis Vassiliki A, Patsoukis Nikolaos
Division of Hematology-Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Immunometabolism. 2022;4(2). doi: 10.20900/immunometab20220007. Epub 2022 Mar 10.
Programmed Death-1 (PD-1; CD279) is an inhibitory receptor induced in several activated immune cells and, after engagement with its ligands PD-L1 and PD-L2, serves as a key mediator of peripheral tolerance. However, PD-1 signaling also has detrimental effects on T cell function by posing breaks on antitumor and antiviral immunity. PD-1 blocking immunotherapy either alone or in combination with other therapeutic modalities has shown great promise in cancer treatment. However, it is unclear why only a small fraction of patients responds to this type of therapy. For this reason, efforts to better understand the mechanisms of PD-1 function have recently been intensified, with the goal to reveal new strategies to overcome current limitations. The signaling pathways that are inhibited by PD-1 impact key regulators of metabolism. Here, we provide an overview of the current knowledge about the effects of PD-1 on metabolic reprogramming of immune cells and their consequences on systemic metabolism.
程序性死亡蛋白 1(PD-1;CD279)是一种在多种活化免疫细胞中诱导产生的抑制性受体,在与配体 PD-L1 和 PD-L2 结合后,作为外周免疫耐受的关键介质。然而,PD-1 信号传导通过对抗肿瘤和抗病毒免疫形成阻碍,也对 T 细胞功能产生有害影响。单独或与其他治疗方式联合使用的 PD-1 阻断免疫疗法在癌症治疗中已显示出巨大潜力。然而,尚不清楚为何只有一小部分患者对这类疗法有反应。因此,最近人们加大了对更好理解 PD-1 功能机制的研究力度,目标是揭示克服当前局限性的新策略。被 PD-1 抑制的信号通路会影响代谢的关键调节因子。在此,我们概述了目前关于 PD-1 对免疫细胞代谢重编程的影响及其对全身代谢后果的认识。