The TNF Receptor Superfamily in Co-stimulating and Co-inhibitory Responses

被引:341
作者
Ward-Kavanagh, Lindsay K. [1 ]
Lin, Wai Wai [1 ]
Sedy, John R. [1 ]
Ware, Carl F. [1 ]
机构
[1] Sanford Burnham Prebys Med Discovery Inst, Infect & Inflammatory Dis Ctr, 10901 North Torrey Pines Rd, La Jolla, CA 92037 USA
关键词
HERPESVIRUS ENTRY MEDIATOR; T-LYMPHOCYTE ATTENUATOR; TUMOR-NECROSIS-FACTOR; GENOME-WIDE ASSOCIATION; KAPPA-B ACTIVATION; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; SYSTEMIC-LUPUS-ERYTHEMATOSUS; GLUCOCORTICOID-INDUCED TNFR; I INTERFERON RESPONSE; VERSUS-HOST-DISEASE;
D O I
10.1016/j.immuni.2016.04.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1005 / 1019
页数:15
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