Schildberg Frank A, Klein Sarah R, Freeman Gordon J, Sharpe Arlene H
Department of Microbiology and Immunobiology, and Evergrande Center for Immunologic Diseases, Harvard Medical School, Boston, MA 02115, USA.
Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Immunity. 2016 May 17;44(5):955-72. doi: 10.1016/j.immuni.2016.05.002.
Immune responses need to be controlled for optimal protective immunity and tolerance. Coinhibitory pathways in the B7-CD28 family provide critical inhibitory signals that regulate immune homeostasis and defense and protect tissue integrity. These coinhibitory signals limit the strength and duration of immune responses, thereby curbing immune-mediated tissue damage, regulating resolution of inflammation, and maintaining tolerance to prevent autoimmunity. Tumors and microbes that cause chronic infections can exploit these coinhibitory pathways to establish an immunosuppressive microenvironment, hindering their eradication. Advances in understanding T cell coinhibitory pathways have stimulated a new era of immunotherapy with effective drugs to treat cancer, autoimmune and infectious diseases, and transplant rejection. In this review we discuss the current knowledge of the mechanisms underlying the coinhibitory functions of pathways in the B7-CD28 family, the diverse functional consequences of these inhibitory signals on immune responses, and the overlapping and unique functions of these key immunoregulatory pathways.
为实现最佳的保护性免疫和耐受性,免疫反应需要得到控制。B7-CD28家族中的共抑制途径提供关键的抑制信号,调节免疫稳态和防御,并保护组织完整性。这些共抑制信号限制免疫反应的强度和持续时间,从而抑制免疫介导的组织损伤,调节炎症的消退,并维持耐受性以预防自身免疫。导致慢性感染的肿瘤和微生物可以利用这些共抑制途径建立免疫抑制微环境,阻碍它们的根除。对T细胞共抑制途径认识的进展激发了免疫治疗的新时代,出现了治疗癌症、自身免疫性疾病、感染性疾病和移植排斥反应的有效药物。在这篇综述中,我们讨论了目前关于B7-CD28家族途径共抑制功能的潜在机制、这些抑制信号对免疫反应的多种功能后果,以及这些关键免疫调节途径的重叠和独特功能的知识。