作者: Arianne C. Richard , John R. Ferdinand , Francoise Meylan , Erika T. Hayes , Odile Gabay
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摘要: Originally described in 2002 as a T cell-costimulatory cytokine, the tumor necrosis factor family member TNF-like 1A (TL1A), encoded by TNFSF15 gene, has since been found to affect multiple cell lineages through its receptor, death receptor 3 (DR3, TNFRSF25) with distinct cell-type effects. Genetic deficiency or blockade of TL1A-DR3 defined number disease states that depend on this cytokine-receptor pair, whereas excess TL1A leads allergic gastrointestinal inflammation stimulation group 2 innate lymphoid cells. Noncoding variants locus are associated susceptibility inflammatory bowel and leprosy, predicting level expression may influence host defense development autoimmune diseases.