Differential expression of GPR15 on T cells during ulcerative colitis

被引:30
作者
Adamczyk, Alexandra [1 ]
Gageik, Daniel [1 ]
Frede, Annika [1 ]
Pastille, Eva [1 ]
Hansen, Wiebke [1 ]
Rueffer, Andreas [2 ]
Buer, Jan [1 ]
Buening, Juergen [3 ]
Langhorst, Jost [4 ]
Westendorf, Astrid M. [1 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Inst Med Microbiol, Essen, Germany
[2] Enterosan, Labor L S, Bad Bocklet, Grobenbrach, Germany
[3] Univ Hosp Schleswig Holstein, Dept Internal Med, Lubeck, Germany
[4] Kliniken Essen Mitte, Ctr Integrat Gastroenterol, Essen, Germany
关键词
INFLAMMATORY-BOWEL-DISEASE; RECEPTOR GPR15; GUT MICROBIOTA; INTESTINE; HOMEOSTASIS; RESPONSES; MUCOSA; COLON;
D O I
10.1172/jci.insight.90585
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
G protein-coupled receptor 15 (GPR15) was recently highlighted as a colon-homing receptor for murine and human CD4(+) T cells. The aim of this study was to explore the functional phenotype of human GPR15(+)CD4(+) T cells, focusing on Tregs and effector T cells (Teffs), and to determine whether GPR15 is the driver for the migration of T cells to the colon during ulcerative colitis (UC). In the peripheral blood, GPR15 was expressed on Tregs and Teffs; both GPR15(+) T cell subsets produced less IFN-gamma and IL-4 but more IL-17 after stimulation and showed a higher migration activity compared with GPR15-CD4(+) T cells. In UC patients, GPR15 expression was increased on Tregs in the peripheral blood but not on Teffs. Interestingly, the expression of GPR15 was significantly enhanced on colonic T cells of UC patients in noninflamed biopsies but not in inflamed biopsies. The differential expression of GPR15 in UC patients was accompanied by a significant reduction of bacterial immunoregulatory metabolites in the feces. In conclusion, GPR15 expression on CD4(+) T cells is altered in UC patients, which may have implications for the development of therapeutic approaches to target T cell trafficking to the colon.
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页数:11
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