Institute of Clinical Chemistry and Pathobiochemistry, School of Medicine, Technical University of Munich, Munich, Germany; Center for Translational Cancer Research (TranslaTUM), Munich, Germany.
Institute of Clinical Chemistry and Pathobiochemistry, School of Medicine, Technical University of Munich, Munich, Germany; Center for Translational Cancer Research (TranslaTUM), Munich, Germany; German Cancer Consortium (DKTK), Heidelberg, Germany; German Center for Infection Research (DZIF), partner site, Munich, Germany.
Trends Immunol. 2019 May;40(5):403-414. doi: 10.1016/j.it.2019.03.005. Epub 2019 Apr 9.
The inhibitory receptor PD-1 is critical to balancing antigen-induced T cell activation; its inhibition is currently being explored to enhance antitumor T cell immunity with certain successful outcomes. However, PD-1 has also emerged as a central tumor suppressor in T cell lymphomas, where the tumor cell originates from a T cell itself. These aggressive cancers are frequently characterized by oncogenic mutations in T cell receptor (TCR) signaling pathways. PD-1 activity within malignant T cells can negatively regulate the PI3K/AKT and PKCθ/NF-κB tumor survival pathways and PD-1 is frequently inactivated in this human malignancy. This review summarizes current insights into oncogenic T cell signaling, discusses tumor-suppressive functions and mechanisms of PD-1 in T cell lymphomagenesis, and addresses potential unwanted effects caused by PD-1 checkpoint inhibition.
抑制性受体 PD-1 对于平衡抗原诱导的 T 细胞激活至关重要;目前正在探索其抑制作用,以增强某些成功结果的抗肿瘤 T 细胞免疫。然而,PD-1 也已成为 T 细胞淋巴瘤中的一个重要肿瘤抑制因子,其中肿瘤细胞源自 T 细胞本身。这些侵袭性癌症通常具有 T 细胞受体 (TCR) 信号通路的致癌突变。恶性 T 细胞内的 PD-1 活性可负调控 PI3K/AKT 和 PKCθ/NF-κB 肿瘤存活途径,并且在这种人类恶性肿瘤中 PD-1 经常失活。本综述总结了目前对致癌 T 细胞信号的认识,讨论了 PD-1 在 T 细胞淋巴瘤发生中的肿瘤抑制功能和机制,并探讨了 PD-1 检查点抑制可能产生的不良影响。