TL1A and DR3, a TNF family ligand-receptor pair that promotes lymphocyte costimulation, mucosal hyperplasia, and autoimmune inflammation

被引:99
|
作者
Meylan, Francoise [1 ]
Richard, Arianne C. [1 ]
Siegel, Richard M. [1 ]
机构
[1] NIAMSD, Immunoregulat Sect, Autoimmun Branch, NIH, Bethesda, MD 20892 USA
关键词
TL1A; DR3; tumor necrosis factor family cytokines; autoimmune disease; inflammatory bowel disease; allergic disease; asthma; DOMAIN-CONTAINING RECEPTOR; IFN-GAMMA PRODUCTION; T-CELL RESPONSES; DEATH-DOMAIN; NKT CELLS; EXPRESSION; TNFRSF25; APOPTOSIS; CYTOKINE; SUSCEPTIBILITY;
D O I
10.1111/j.1600-065X.2011.01068.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DR3 (TNFRSF25) is a member of the tumor necrosis factor receptor (TNFR) superfamily expressed primarily on lymphocytes and is a receptor for the TNF family cytokine TL1A (TNFSF15). DR3 costimulates T-cell activation, but it is unique among these receptors in that it signals through an intracytoplasmic death domain and the adapter protein TRADD (TNFR-associated death domain). TL1A costimulates T cells to produce a wide variety of cytokines and can promote expansion of activated and regulatory T cells in vivo. Studies in mice deficient in DR3 or TL1A or in animals treated with antibodies that block the activity of TL1A have revealed a specific role for DR3 in enhancing effector T-cell proliferation at the site of tissue inflammation in autoimmune disease models. DR3 appears to be required in autoimmune disease models dependent on a variety of different T-cell subsets and also invariant natural killer T (iNKT) cells. Chronic expression of TL1A induces a distinct interleukin-13-dependent pathology in the small intestine marked by goblet cell hyperplasia and other features associated with allergic and anti-parasitic responses. These studies suggest that TL1A may be a viable target for therapies designed to inhibit the T-cell-dependent component of diverse autoimmune diseases.
引用
收藏
页码:188 / 196
页数:9
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