Flow cytometric analysis of expression of transforming growth factor-β and glucocorticoid-induced tumor necrosis factor receptor on CD4+CD25+T cells of patients with inflammatory bowel disease

被引:18
作者
Ikeda, M
Takeshima, F
Ohba, K
Ohnita, K
Isomoto, H
Yamakawa, M
Omagari, K
Mizuta, Y
Kohno, S
机构
[1] Nagasaki Univ, Sch Med, Dept Gen Med, Nagasaki 8528501, Japan
[2] Nagasaki Univ, Sch Med, Dept Internal Med 2, Nagasaki 8528501, Japan
[3] Nagasaki Municipal Hosp, Dept Internal Med, Nagasaki, Japan
关键词
inflammatory bowel disease; regulatory T cell; transforming growth factor-beta;
D O I
10.1007/s10620-006-3105-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To determine whether human CD4+CD25+ cells express glucocorticoid-induced tumor necrosis factor receptor (GITR) and transforming growth factor-beta (TGF-beta) and the difference in CD4+CD25+ cells between patients with inflammatory bowel diseases and healthy subjects, peripheral blood lymphocytes were obtained from patients with ulcerative colitis (UC; n = 50), Crohn's disease (CD; n = 49), and healthy volunteers (control; n = 50) and flow cytometric analysis was performed. In control subjects, the expression of GITR on CD4+CD25+ cells (41.8 +/- 10.5%) was significantly higher than on CD4+CD25- cells (11.1 +/- 7.4%). Similarly, TGF-beta expression on CD4+CD25+ cells (5.3 +/- 4.6%) was higher than on CD4+CD25- cells (1.2 +/- 1.4%). There were no significant differences among UC, CD, and control in CD4+CD25+/CD4+ ratio. However, there was a significant difference in the CD4+CD25+TGF-beta+/CD4+CD25+ ratio between active UC and inactive UC (2.7 +/- 2.6 and 7.2 +/- 3.9%, respectively). The results suggest that TGF-beta is involved in the induction or sustained remission of UC.
引用
收藏
页码:178 / 184
页数:7
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