免疫系统
免疫原性细胞死亡
免疫疗法
封锁
医学
化疗
免疫抑制
肿瘤微环境
免疫检查点
癌症研究
T细胞
免疫学
获得性免疫系统
肺癌
抗原
程序性细胞死亡
肿瘤科
生物
细胞凋亡
内科学
受体
生物化学
作者
Matthen Mathew,Thomas Enzler,Catherine A. Shu,Naiyer A. Rizvi
标识
DOI:10.1016/j.pharmthera.2018.01.003
摘要
Antitumor immunity relies on the ability of the immune system to recognize tumor cells as foreign and eliminate them. An effective immune response in this setting is due to surveillance of tumor-specific antigens that induce an adaptive immune response resulting in T-cell mediated cytotoxicity. Immune checkpoint inhibitors, specifically those targeting the programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) axis, have demonstrated promising activity in non-small cell lung cancer (NSCLC). However, there remains a crucial need for better treatment strategies for the majority of patients with advanced NSCLC, particularly in the frontline setting. Chemotherapy can increase antigenicity via immunogenic cell death (ICD) of tumor cells as well as also reduce “off target” immunosuppression in the tumor microenvironment (TME). Combining chemotherapy with PD-1 blockade harnesses the potential synergy between these agents and has led to encouraging results in the up-front treatment of NSCLC. In this review, we summarize the preclinical rationale behind these combinations and review recent trial data demonstrating their efficacy.
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