Regulatory T cells in type 1 diabetic patients with autoimmune chronic atrophic gastritis

Endocrine. 2009 Jun;35(3):420-8. doi: 10.1007/s12020-009-9166-2. Epub 2009 Mar 17.

Abstract

Type A chronic atrophic gastritis (CAG) is increased in type 1 diabetic patients (DM1). To address this issue, we determined and analyzed the number of peripheral blood regulatory T cells (Tregs) in 15 DM1-CAG patients, 15 DM1 patients without associated autoantibodies (DM1) and 15 healthy controls by flow cytometry and compared gastric Tregs expression (CD4+Foxp3+/CD4+) in DM1-CAG patients with that observed in 10 control Helicobacter pylori CAG-infected biopsies. The percentage of peripheral Tregs was higher in DM1-CAG patients compared to DM1 and controls (CD4+Foxp3+: 7.67 +/- 1.91% vs. 5.38 +/- 1.57% and 5.65 +/- 1.76%, P < 0.001, respectively), with no differences between DM1 and controls. Gastric mucosal Tregs were higher in H. pylori CAG than in DM1-CAG patients (31.31 +/- 5.52% vs. 7.68 +/- 3.70%; P < 0.001). Data suggest that Tregs are stimulated in patients with more than one autoimmune disease (DM1 + CAG) in an ineffectual attempt to control autoimmune response and that the number of Tregs in gastric mucosa implicated in the chronification of gastritis differs according to the etiology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Autoimmune Diseases / complications
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • Case-Control Studies
  • Diabetes Mellitus, Type 1 / complications*
  • Diabetes Mellitus, Type 1 / immunology*
  • Diabetes Mellitus, Type 1 / pathology
  • Female
  • Forkhead Transcription Factors / metabolism
  • Gastric Mucosa / immunology
  • Gastric Mucosa / metabolism
  • Gastric Mucosa / pathology
  • Gastritis, Atrophic / complications*
  • Gastritis, Atrophic / immunology
  • Gastritis, Atrophic / metabolism
  • Gastritis, Atrophic / pathology
  • Humans
  • Male
  • Middle Aged
  • T-Lymphocytes, Regulatory / pathology*
  • Young Adult

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors