Gastric T lymphocyte responses to Helicobacter pylori in patients with H pylori colonisation

Gut. 1994 Oct;35(10):1379-84. doi: 10.1136/gut.35.10.1379.

Abstract

Helicobacter pylori has been identified as a dominant factor in the pathogenesis of duodenal ulcer. The aim of this study was to examine peripheral blood and gastric lymphocyte proliferation and cytokine production in patients with H pylori colonisation. Sixty five dyspeptic patients attending for endoscopy were studied; 35 of these were H pylori positive and 30 H pylori negative as assessed by culture, histology, and rapid urease test. H pylori antigen was capable of stimulating peripheral blood lymphocyte proliferative responses even in H pylori negative patients. Peripheral blood lymphocyte proliferative responses to H pylori (but not to purified protein derivative or phythaemagglutinin) were significantly lower in H pylori positive than H pylori negative patients. Similarly, antigen specific proliferative responses and interferon gamma production by gastric lamina propria lymphocytes were also depressed in H pylori positive patients compared with H pylori negative patients. CD8 and CD22 positive lamina propria lymphocytes were increased in H pylori positive patients. These data show that antigen specific responses to H pylori are significantly lower in H pylori positive patients and could indicate activation of antigen specific suppression.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigen-Presenting Cells / immunology
  • Antigens, Bacterial / immunology
  • Cells, Cultured
  • Cytokines / metabolism
  • Female
  • Helicobacter Infections / blood
  • Helicobacter Infections / immunology*
  • Helicobacter pylori / immunology*
  • Humans
  • Immunophenotyping
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / pharmacology
  • Lymphocyte Activation*
  • Male
  • Middle Aged
  • Stomach / immunology*
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Antigens, Bacterial
  • Cytokines
  • Interleukin-2
  • Interferon-gamma