Ward-Kavanagh Lindsay K, Lin Wai Wai, Šedý John R, Ware Carl F
Infectious and Inflammatory Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Infectious and Inflammatory Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Immunity. 2016 May 17;44(5):1005-19. doi: 10.1016/j.immuni.2016.04.019.
Cytokines related to tumor necrosis factor (TNF) provide a communication network essential for coordinating multiple cell types into an effective host defense system against pathogens and malignant cells. The pathways controlled by the TNF superfamily differentiate both innate and adaptive immune cells and modulate stromal cells into microenvironments conducive to host defenses. Members of the TNF receptor superfamily activate diverse cellular functions from the production of type 1 interferons to the modulation of survival of antigen-activated T cells. Here, we focus attention on the subset of TNF superfamily receptors encoded in the immune response locus in chromosomal region 1p36. Recent studies have revealed that these receptors use diverse mechanisms to either co-stimulate or restrict immune responses. Translation of the fundamental mechanisms of TNF superfamily is leading to the design of therapeutics that can alter pathogenic processes in several autoimmune diseases or promote immunity to tumors.
与肿瘤坏死因子(TNF)相关的细胞因子提供了一个通信网络,这对于将多种细胞类型协调成一个有效的宿主防御系统以抵御病原体和恶性细胞至关重要。由TNF超家族控制的信号通路可区分先天性和适应性免疫细胞,并将基质细胞调节到有利于宿主防御的微环境中。TNF受体超家族的成员激活了从1型干扰素的产生到抗原激活的T细胞存活调节等多种细胞功能。在这里,我们将注意力集中在染色体区域1p36免疫反应基因座中编码的TNF超家族受体子集上。最近的研究表明,这些受体使用多种机制来共同刺激或限制免疫反应。对TNF超家族基本机制的解读正在引领治疗药物的设计,这些药物可以改变几种自身免疫性疾病的致病过程或增强对肿瘤的免疫力。