Digestive Diseases and Sciences

, Volume 52, Issue 10, pp 2725–2731

Demonstration of Low-Regulatory CD25High+CD4+ and High-Pro-inflammatory CD28CD4+ T-Cell Subsets in Patients with Ulcerative Colitis: Modified by Selective Granulocyte and Monocyte Adsorption Apheresis

Authors

  • Yoko Yokoyama
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Yoshihiro Fukuda
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Katsuyuki Tozawa
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Koji Kamikozuru
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Kunio Ohnishi
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Takeshi Kusaka
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Tadashi Kosaka
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Nobuyuki Hida
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Yoshio Ohda
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
  • Hiroto Miwa
    • Division of Upper Gastroenterology, Department of Internal MedicineHyogo College of Medicine
  • Takayuki Matsumoto
    • Division of Lower GastroenterologyDepartment of Internal Medicine, Hyogo College of Medicine
Original Article

DOI: 10.1007/s10620-006-9560-z

Cite this article as:
Yokoyama, Y., Fukunaga, K., Fukuda, Y. et al. Dig Dis Sci (2007) 52: 2725. doi:10.1007/s10620-006-9560-z

Abstract

Low-CD25High+CD4+, a subset of regulatory CD25+CD4+ T cells and high-inflammatory CD28CD4+ T cells can exacerbate ulcerative colitis (UC). This study sought to investigate the frequency of CD25High+CD4+ and CD28CD4+ T cells in patients with UC and the changes in these cells during Adacolumn granulocyte and monocyte adsorption apheresis (GMA). Subjects were 12 patients with active UC, 11 with quiescent UC, and 14 healthy volunteers (HVs). The mean clinical activity index was 15.7 ± 2.2 in active UC and 4.5 ± 1.1 in quiescent UC. Peripheral blood samples were stained with CD4, CD25, and CD28 antibodies for flow cytometry. Patients with active UC received GMA and blood samples were examined before and after the first GMA session. Patients with active UC (P < 0.04) or quiescent UC (P < 0.02) had a higher percentage of CD28D4+T cells compared with HVs, while the percentage of CD28+CD4+ T cells was lower in both UC groups compared with HVs (P = 0.03 and P < 0.02). Patients with active UC had a lower percentage of CD25High+CD4+T cells compared with quiescent UC patients (P < 0.001). A significant increase in CD25High+CD4+ T cells was associated with GMA (P < 0.03). Low CD25High+CD4+ and high CD28CD4+ are prominent features in UC. The increase in CD25High+CD4+ T cells induced by GMA should contribute to improved immune function. Additional studies are warranted, since a low frequency of CD25High+CD4+ and a high frequency of CD28CD4+ expressing T cells might be a predictor of clinical response to GMA.

Keywords

Ulcerative colitis Regulatory T cells CD25High+CD4+ CD28+CD4+ CD28CD4 Granulocyte and monocyte apheresis

Copyright information

© Springer Science+Business Media, Inc. 2006