免疫学
生物
肿瘤坏死因子α
细胞因子
先天性淋巴细胞
炎症性肠病
先天免疫系统
疾病
免疫系统
医学
内科学
作者
Arianne C. Richard,John R. Ferdinand,Françoise Meylan,Erika Hayes,Odile Gabay,Richard M. Siegel
标识
DOI:10.1189/jlb.3ri0315-095r
摘要
Abstract Originally described in 2002 as a T cell-costimulatory cytokine, the tumor necrosis factor family member TNF-like factor 1A (TL1A), encoded by the TNFSF15 gene, has since been found to affect multiple cell lineages through its receptor, death receptor 3 (DR3, encoded by TNFRSF25) with distinct cell-type effects. Genetic deficiency or blockade of TL1A-DR3 has defined a number of disease states that depend on this cytokine-receptor pair, whereas excess TL1A leads to allergic gastrointestinal inflammation through stimulation of group 2 innate lymphoid cells. Noncoding variants in the TL1A locus are associated with susceptibility to inflammatory bowel disease and leprosy, predicting that the level of TL1A expression may influence host defense and the development of autoimmune and inflammatory diseases.
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