Chronic mucosal inflammation of the gastric cardia in gastroesophageal reflux disease is not regulated by FOXP3-expressing T cells

Dig Dis Sci. 2009 Sep;54(9):1940-6. doi: 10.1007/s10620-009-0746-z. Epub 2009 Feb 26.

Abstract

Introduction: Chronic inflammation at the cardia occurs in gastroesophageal reflux disease (GERD), as well as in the presence of Helicobacter pylori. Regulatory T cells have been demonstrated for H. pylori-induced gastritis, whereas their role has not been studied in GERD.

Methods: We prospectively analyzed the expression of FOXP3, a marker of various regulatory T cells, as well as the mucosal transcript levels of TGF-beta1 and IL-10. RNA and protein levels have been determined in cardiac biopsies of 70 patients stratified according to GERD (n = 22), controls (n = 17), and H. pylori (n = 31).

Results: GERD presented with chronic inflammation and reduced FOXP3-mRNA in the cardiac mucosa (-84%), whereas H. pylori-positive patients revealed a 25.1-fold increase of FOXP3 gene expression. These results were verified by the regulatory cytokines IL-10 and TGF-beta1, and by the immunohistochemical detection of intramucosal FOXP3-expressing T cells.

Conclusion: Chronic inflammation at the cardia associated with either GERD or H. pylori differs concerning the presence of FOXP3-expressing T cells. In contrast to H. pylori, FOXP3-expressing T cells are not associated with GERD-associated carditis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cardia / metabolism*
  • Cardia / pathology
  • Female
  • Forkhead Transcription Factors / metabolism*
  • Gastric Mucosa / immunology
  • Gastric Mucosa / metabolism
  • Gastritis / immunology*
  • Gastritis / metabolism
  • Gastritis / pathology
  • Gastroesophageal Reflux / complications
  • Gastroesophageal Reflux / immunology*
  • Gastroesophageal Reflux / metabolism
  • Gastroesophageal Reflux / pathology
  • Gene Expression
  • Humans
  • Interleukin-10 / metabolism
  • Male
  • Middle Aged
  • Prospective Studies
  • T-Lymphocytes, Regulatory / metabolism*
  • Transforming Growth Factor beta1 / metabolism
  • Young Adult

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Transforming Growth Factor beta1
  • Interleukin-10