Department of Infection and Immunity, Experimental and Molecular Immunology, Luxembourg Institute of Health, Esch-sur-Alzette, Luxembourg ; Odense Research Center for Anaphylaxis, Department of Dermatology and Allergy Center, Odense University Hospital, University of Southern Denmark , Odense , Denmark ; and Life Sciences Research Unit, Molecular Disease Mechanisms Group, University of Luxembourg, Belvaux, Luxembourg.
Physiol Rev. 2019 Jan 1;99(1):115-160. doi: 10.1152/physrev.00045.2017.
The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and stimulus-responsive processes in vivo. TNFSF/TNFRSF members regulate cellular differentiation, survival, and programmed death, but their most critical functions pertain to the immune system. Both innate and adaptive immune cells are controlled by TNFSF/TNFRSF members in a manner that is crucial for the coordination of various mechanisms driving either co-stimulation or co-inhibition of the immune response. Dysregulation of these same signaling pathways has been implicated in inflammatory and autoimmune diseases, highlighting the importance of their tight regulation. Investigation of the control of TNFSF/TNFRSF activities has led to the development of therapeutics with the potential to reduce chronic inflammation or promote anti-tumor immunity. The study of TNFSF/TNFRSF proteins has exploded over the last 30 yr, but there remains a need to better understand the fundamental mechanisms underlying the molecular pathways they mediate to design more effective anti-inflammatory and anti-cancer therapies.
肿瘤坏死因子 (TNF) 和 TNF 受体 (TNFR) 超家族 (TNFSF/TNFRSF) 包括 19 种配体和 29 种受体,它们在调节细胞功能方面发挥着重要作用。TNFSF/TNFRSF 介导的通讯途径对于体内众多发育、动态平衡和刺激反应过程至关重要。TNFSF/TNFRSF 成员调节细胞分化、存活和程序性死亡,但它们最关键的功能与免疫系统有关。先天和适应性免疫细胞都受到 TNFSF/TNFRSF 成员的控制,这种控制对于协调各种驱动免疫反应协同刺激或协同抑制的机制至关重要。这些相同信号通路的失调与炎症和自身免疫性疾病有关,强调了其严密调控的重要性。对 TNFSF/TNFRSF 活性的控制的研究导致了具有潜在减少慢性炎症或促进抗肿瘤免疫的治疗方法的发展。TNFSF/TNFRSF 蛋白的研究在过去 30 年中爆发式增长,但仍需要更好地了解它们介导的分子途径的基本机制,以设计更有效的抗炎和抗癌疗法。