Wang Yifan, Deng Weiye, Li Nan, Neri Shinya, Sharma Amrish, Jiang Wen, Lin Steven H
Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, United States.
Front Pharmacol. 2018 Mar 5;9:185. doi: 10.3389/fphar.2018.00185. eCollection 2018.
Since the approval of anti-CTLA4 therapy (ipilimumab) for late-stage melanoma in 2011, the development of anticancer immunotherapy agents has thrived. The success of many immune-checkpoint inhibitors has drastically changed the landscape of cancer treatment. For some types of cancer, monotherapy for targeting immune checkpoint pathways has proven more effective than traditional therapies, and combining immunotherapy with current treatment strategies may yield even better outcomes. Numerous preclinical studies have suggested that combining immunotherapy with radiotherapy could be a promising strategy for synergistic enhancement of treatment efficacy. Radiation delivered to the tumor site affects both tumor cells and surrounding stromal cells. Radiation-induced cancer cell damage exposes tumor-specific antigens that make them visible to immune surveillance and promotes the priming and activation of cytotoxic T cells. Radiation-induced modulation of the tumor microenvironment may also facilitate the recruitment and infiltration of immune cells. This unique relationship is the rationale for combining radiation with immune checkpoint blockade. Enhanced tumor recognition and immune cell targeting with checkpoint blockade may unleash the immune system to eliminate the cancer cells. However, challenges remain to be addressed to maximize the efficacy of this promising combination. Here we summarize the mechanisms of radiation and immune system interaction, and we discuss current challenges in radiation and immune checkpoint blockade therapy and possible future approaches to boost this combination.
自2011年抗CTLA4疗法(伊匹单抗)获批用于晚期黑色素瘤治疗以来,抗癌免疫治疗药物的研发蓬勃发展。许多免疫检查点抑制剂的成功应用极大地改变了癌症治疗的格局。对于某些类型的癌症,靶向免疫检查点通路的单药治疗已被证明比传统疗法更有效,将免疫疗法与当前治疗策略相结合可能会产生更好的效果。大量临床前研究表明,将免疫疗法与放射疗法相结合可能是一种有前景的协同增强治疗效果的策略。照射到肿瘤部位的辐射会影响肿瘤细胞和周围的基质细胞。辐射诱导的癌细胞损伤会暴露肿瘤特异性抗原,使其能够被免疫监视识别,并促进细胞毒性T细胞的致敏和激活。辐射诱导的肿瘤微环境调节也可能促进免疫细胞的募集和浸润。这种独特的关系是将放疗与免疫检查点阻断相结合的理论基础。通过检查点阻断增强肿瘤识别和免疫细胞靶向作用,可能会释放免疫系统来消除癌细胞。然而,要使这种有前景的联合治疗效果最大化,仍有一些挑战有待解决。在此,我们总结了辐射与免疫系统相互作用的机制,并讨论了放疗和免疫检查点阻断治疗当前面临的挑战以及未来可能增强这种联合治疗效果的方法。