Chair of Pharmacology, Faculty of Science, University of Fribourg, 1700, Fribourg, Switzerland; Institute of Pharmaceutical Sciences, University of Geneva, University of Lausanne, 1211, Geneva, Switzerland; Department of Anesthesiology, Pharmacology and Intensive Care, Faculty of Medicine, University of Geneva, 1211, Geneva, Switzerland.
Institute of Pharmaceutical Sciences, University of Geneva, University of Lausanne, 1211, Geneva, Switzerland.
Pharmacol Res. 2020 Apr;154:104192. doi: 10.1016/j.phrs.2019.03.001. Epub 2019 Mar 2.
Cancer immunotherapy has come of age with the advent of immune checkpoint inhibitors. In this article we review how agonists for receptors of the innate immune system, the Toll-like receptors and the RIG-I-like receptors, impact anticancer immune responses. Treatment with these agonists enhances the activity of anticancer effector cells, such as cytotoxic T cells and NK cells, and at the same time blocks the activity of immunosuppressive cell types such as regulatory T cells and myeloid-derived suppressor cells. These compounds also impact the recruitment of immune cells to the tumor. The phenomena of pattern-recognition receptor tolerance and reprogramming and their implications for immunotherapy are discussed. Finally, novel delivery systems that target the immune-stimulating drugs to the tumor or the tumor-draining lymph nodes to enhance their efficacy and safety are presented.
癌症免疫疗法随着免疫检查点抑制剂的出现而成熟。在本文中,我们回顾了先天免疫受体激动剂,如 Toll 样受体和 RIG-I 样受体,如何影响抗肿瘤免疫反应。这些激动剂的治疗增强了抗肿瘤效应细胞的活性,如细胞毒性 T 细胞和 NK 细胞,同时抑制了免疫抑制细胞类型的活性,如调节性 T 细胞和髓系来源的抑制细胞。这些化合物还影响免疫细胞向肿瘤的募集。讨论了模式识别受体耐受和重编程的现象及其对免疫治疗的影响。最后,提出了将免疫刺激药物靶向肿瘤或肿瘤引流淋巴结以增强其疗效和安全性的新型递药系统。