In situ correlation of cytokine secretion and apoptosis in Helicobacter pylori-associated gastritis

Am J Physiol Gastrointest Liver Physiol. 2002 Aug;283(2):G481-8. doi: 10.1152/ajpgi.00422.2001.

Abstract

Tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) are important for the pathogenesis of Helicobacter pylori-associated gastritis and peptic ulcer disease. Gastric biopsies from H. pylori-positive and -negative patients were used to examine the in situ correlation of TNF-alpha and IFN-gamma with epithelial cell apoptosis, bacterial load, and histological parameters of gastritis. From the same patients, we isolated H. pylori-specific T cell lines and clones and examined their ex vivo release of proinflammatory cytokines. We found a highly significant correlation of TNF-alpha and IFN-gamma production with activity and grade of gastritis (P < 0.01), H. pylori density (P = 0.01), epithelial cell apoptosis (P < 0.001), and Fas/Fas-ligand expression (P < 0.001). T cell lines and clones were all TCR-alphabeta(+) and showed T helper 1 functional phenotype. With the use of serial histological sections, this study showed for the first time the in situ correlation of TNF-alpha and IFN-gamma with epithelial cell apoptosis, bacterial load, and histological severity of disease and emphasizes the role of these cytokines in the pathophysiology of H. pylori-associated disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Apoptosis*
  • Cell Line
  • Clone Cells
  • Cytokines / metabolism*
  • Fas Ligand Protein
  • Gastric Mucosa / metabolism
  • Gastritis / microbiology*
  • Gastritis / pathology
  • Gastritis / physiopathology*
  • HLA-DR Antigens / metabolism
  • Helicobacter Infections*
  • Helicobacter pylori*
  • Humans
  • Interferon-gamma / metabolism
  • Membrane Glycoproteins / metabolism
  • Middle Aged
  • Stomach / pathology
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / pathology
  • Tumor Necrosis Factor-alpha / metabolism
  • fas Receptor / metabolism

Substances

  • Cytokines
  • FASLG protein, human
  • Fas Ligand Protein
  • HLA-DR Antigens
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Interferon-gamma