固有层
溃疡性结肠炎
炎症性肠病
细胞因子
肿瘤坏死因子α
外周血单个核细胞
免疫学
CD8型
炎症
医学
生物
疾病
内科学
病理
免疫系统
体外
上皮
生物化学
作者
Giorgos Bamias,Charles T. Martin,Marco Marini,Sharon B. Hoang,Margarita Mishina,William G. Ross,Muhammadreza A. Sachedina,Charles M. Friel,James Mize,Stephen J. Bickston,Theresa T. Pizarro,Ping Wei,Fabio Cominelli
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2003-11-01
卷期号:171 (9): 4868-4874
被引量:299
标识
DOI:10.4049/jimmunol.171.9.4868
摘要
TL1A is a novel TNF-like factor that acts as a costimulator of IFN-gamma secretion through binding to the death domain-containing receptor, DR3. The aim of this study was to test the hypothesis that TL1A may play an important role in inflammatory bowel disease (IBD) by functioning as a Th1-polarizing cytokine. The expression, cellular localization, and functional activity of TL1A and DR3 were studied in intestinal tissue specimens as well as isolated lamina propria mononuclear cells from IBD patients and controls. TL1A mRNA and protein expression was up-regulated in IBD, particularly in involved areas of Crohn's disease (CD; p < 0.03 vs control). TL1A production was localized to the intestinal lamina propria in macrophages and CD4(+) and CD8(+) lymphocytes from CD patients as well as in plasma cells from ulcerative colitis patients. The amount of TL1A protein and the number of TL1A-positive cells correlated with the severity of inflammation, most significantly in CD. Increased numbers of immunoreactive DR3-positive T lymphocytes were detected in the intestinal lamina propria from IBD patients. Addition of recombinant human TL1A to cultures of PHA-stimulated lamina propria mononuclear from CD patients significantly augmented IFN-gamma production by 4-fold, whereas a minimal effect was observed in control patients. Our study provides evidence for the first time that the novel cytokine TL1A may play an important role in a Th1-mediated disease such as CD.
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