Swart Maarten, Verbrugge Inge, Beltman Joost B
Division of Toxicology, Leiden Academic Centre for Drug Research, Leiden University , Leiden , Netherlands.
Division of Immunology, Netherlands Cancer Institute , Amsterdam , Netherlands.
Front Oncol. 2016 Nov 1;6:233. doi: 10.3389/fonc.2016.00233. eCollection 2016.
In healthy individuals, immune-checkpoint molecules prevent autoimmune responses and limit immune cell-mediated tissue damage. Tumors frequently exploit these molecules to evade eradication by the immune system. Over the past years, immune-checkpoint blockade of cytotoxic T lymphocyte antigen-4 and programed death-1 emerged as promising strategies to activate antitumor cytotoxic T cell responses. Although complete regression and long-term survival is achieved in some patients, not all patients respond. This review describes promising, novel combination approaches involving immune-checkpoint blockade in the context of the cancer-immunity cycle, aimed at increasing response rates to the single treatments. Specifically, we discuss combinations that promote antigen release and presentation, that further amplify T cell activation, that inhibit trafficking of regulatory T cells or MSDCs, that stimulate intratumoral T cell infiltration, that increase cancer recognition by T cells, and that stimulate tumor killing.
在健康个体中,免疫检查点分子可预防自身免疫反应并限制免疫细胞介导的组织损伤。肿瘤常常利用这些分子来逃避免疫系统的清除。在过去几年中,细胞毒性T淋巴细胞抗原4和程序性死亡1的免疫检查点阻断已成为激活抗肿瘤细胞毒性T细胞反应的有前景的策略。尽管一些患者实现了完全缓解和长期生存,但并非所有患者都有反应。本综述描述了在癌症免疫循环背景下涉及免疫检查点阻断的有前景的新型联合方法,旨在提高对单一治疗的反应率。具体而言,我们讨论了促进抗原释放和呈递、进一步放大T细胞活化、抑制调节性T细胞或髓样来源的抑制性细胞的迁移、刺激肿瘤内T细胞浸润、增加T细胞对癌症的识别以及刺激肿瘤杀伤的联合方法。