Jeong Seongju, Park Su-Hyung
Biomedical Science and Engineering Interdisciplinary Program, KAIST, Daejeon 34141, Korea.
Laboratory of Translational Immunology and Vaccinology, Graduate School of Medical Science and Engineering, KAIST, Daejeon 34141, Korea.
Immune Netw. 2020 Feb 7;20(1):e3. doi: 10.4110/in.2020.20.e3. eCollection 2020 Feb.
Immune checkpoint inhibitors (ICIs), including anti-PD-1 and anti-CTLA-4 therapeutic agents, are now approved by the Food and Drug Administration for treatment of various types of cancer. However, the therapeutic efficacy of ICIs varies among patients and cancer types. Moreover, most patients do not develop durable antitumor responses after ICI therapy due to an ephemeral reversal of T-cell dysfunction. As co-stimulatory receptors play key roles in regulating the effector functions of T cells, activating co-stimulatory pathways may improve checkpoint inhibition efficacy, and lead to durable antitumor responses. Here, we review recent advances in our understating of co-stimulatory receptors in cancers, providing the necessary groundwork for the rational design of cancer immunotherapy.
免疫检查点抑制剂(ICI),包括抗程序性死亡蛋白1(PD-1)和抗细胞毒性T淋巴细胞相关蛋白4(CTLA-4)治疗药物,目前已获美国食品药品监督管理局批准用于治疗多种类型的癌症。然而,ICI的治疗效果在患者和癌症类型之间存在差异。此外,由于T细胞功能障碍的短暂逆转,大多数患者在ICI治疗后并未产生持久的抗肿瘤反应。由于共刺激受体在调节T细胞的效应功能中起关键作用,激活共刺激途径可能会提高检查点抑制疗效,并导致持久的抗肿瘤反应。在此,我们综述了近期在理解癌症中共刺激受体方面取得的进展,为癌症免疫治疗的合理设计提供必要的基础。