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TL1A exerts pleiotropic effects on cell proliferation, activation, and differentiation of immune cells, including helper T cells and regulatory T cells. TL1A and its two receptors expression is increased in both serum and inflamed tissues in autoimmune diseases such as inflammatory bowel disease (IBD), rheumatoid arthritis (RA), and ankylosing spondylitis (AS). Polymorphisms of the\n                    <jats:italic>TNFSF15<\/jats:italic>\n                    gene that encodes TL1A are associated with the pathogenesis of irritable bowel syndrome, leprosy, and autoimmune diseases, including IBD, AS, and primary biliary cirrhosis (PBC). In mice, blocking of TL1A-DR3 interaction by either antagonistic antibodies or deletion of the DR3 gene attenuates the severity of multiple autoimmune diseases, whereas sustained TL1A expression on T cells or dendritic cells induces IL-13-dependent small intestinal inflammation. This suggests that modulation of TL1A-DR3 interaction may be a potential therapeutic target in several autoimmune diseases, including IBD, RA, AS, and PBC.\n                  <\/jats:p>","DOI":"10.1155\/2013\/258164","type":"journal-article","created":{"date-parts":[[2013,12,21]],"date-time":"2013-12-21T16:00:43Z","timestamp":1387641643000},"page":"1-9","source":"Crossref","is-referenced-by-count":60,"title":["The Role of TL1A and DR3 in Autoimmune and Inflammatory Diseases"],"prefix":"10.1155","volume":"2013","author":[{"given":"Yoshihiro","family":"Aiba","sequence":"first","affiliation":[{"name":"Clinical Research Center, National Hospital Organization Nagasaki Medical Center, Kubara 2-1001-1, Omura 856-8562, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Minoru","family":"Nakamura","sequence":"additional","affiliation":[{"name":"Clinical Research Center, National Hospital Organization Nagasaki Medical Center, Kubara 2-1001-1, Omura 856-8562, 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