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
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作者:
Maho Ikeda
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Maho Ikeda
Fuminao Takeshima
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Fuminao Takeshima
Kazuo Ohba
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Kazuo Ohba
Ken Ohnita
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Ken Ohnita
Hajime Isomoto
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Hajime Isomoto
Masaki Yamakawa
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Masaki Yamakawa
Katsuhisa Omagari
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Katsuhisa Omagari
Yohei Mizuta
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Yohei Mizuta
Shigeru Kohno
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机构:Nagasaki University School of Medicine,Second Department of Internal Medicine
Shigeru Kohno
机构:
[1] Nagasaki University School of Medicine,Second Department of Internal Medicine
[2] Nagasaki University School of Medicine,Department of General Medicine
[3] Nagasaki Municipal Hospital,Department of Internal Medicine
[4] Nagasaki University School of Medicine,Department of General Medicine
inflammatory bowel disease;
regulatory T cell;
transforming growth factor-β;
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摘要:
To determine whether human CD4+CD25+ cells express glucocorticoid-induced tumor necrosis factor receptor (GITR) and transforming growth factor-β (TGF-β) 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-β 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-β+/CD4+CD25+ ratio between active UC and inactive UC (2.7 ± 2.6 and 7.2 ± 3.9%, respectively). The results suggest that TGF-β is involved in the induction or sustained remission of UC.
机构:
Univ So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USAUniv So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USA
Watanabe, M
Mencel, RL
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Univ So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USAUniv So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USA
Mencel, RL
Cramer, DV
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机构:
Univ So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USAUniv So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USA
Cramer, DV
Starnes, VA
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机构:
Univ So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USAUniv So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USA
Starnes, VA
Barr, ML
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机构:
Univ So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USAUniv So Calif, Childrens Hosp Los Angeles, Dept Cardiothorac Surg, Los Angeles, CA 90027 USA
Barr, ML
[J].
JOURNAL OF HEART AND LUNG TRANSPLANTATION,
2005,
24
(12):
: 2153
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2159