Suppression of human mononuclear cell response by Helicobacter pylori: effects on isolated monocytes and lymphocytes

FEMS Immunol Med Microbiol. 1994 Feb;8(2):157-66. doi: 10.1111/j.1574-695X.1994.tb00438.x.


Helicobacter pylori colonization of the human gastric mucosa causes a long-term, not self-limiting inflammation, suggesting that the microbe has properties to protect itself against the host immune defence system. Recently we were able to demonstrate that H. pylori suppresses the in vitro proliferative response of human peripheral blood mononuclear cells to antigens as well as to mitogens without affecting cell viability. The purpose of this study was to clarify which cell subsets of mononuclear cells are influenced by H. pylori. The use of monocytes which had been pretreated with a soluble cytoplasmic fraction of H. pylori (30 micrograms ml-1) led to a suppressed proliferation of T cells after PHA-activation. Activation of isolated T cells with PHA and PMA revealed that the proliferative response of lymphocytes could also be inhibited independently of monocytes. The anti-proliferative effect was associated with a reduction of IL-2 receptor (CD25) expression as well as an inhibition of blastogenesis. Furthermore, the spontaneous proliferation of EBV-transformed B cell lines was suppressed in a dose-dependent manner. FACS-analysis of HLA-DR, ICAM-1 and CD14 expression on the surface of monocytes revealed an influence of H. pylori on CD14 expression at a concentration of 30 micrograms ml-1, while the expression of HLA-DR and ICAM-1 was not affected at this concentration.

MeSH terms

  • Antigens, CD / biosynthesis
  • Antigens, Surface / biosynthesis
  • B-Lymphocytes / immunology
  • Cell Adhesion Molecules / biosynthesis
  • Cell Transformation, Viral
  • Cytoplasm / immunology
  • HLA-DR Antigens / biosynthesis
  • Helicobacter pylori / immunology*
  • Humans
  • Immune Tolerance / immunology
  • In Vitro Techniques
  • Intercellular Adhesion Molecule-1
  • Lymphocyte Activation / drug effects
  • Monocytes / immunology*
  • Phytohemagglutinins / pharmacology
  • Subcellular Fractions / immunology
  • T-Lymphocytes / immunology*
  • Tetradecanoylphorbol Acetate / pharmacology


  • Antigens, CD
  • Antigens, Surface
  • Cell Adhesion Molecules
  • HLA-DR Antigens
  • Phytohemagglutinins
  • Intercellular Adhesion Molecule-1
  • Tetradecanoylphorbol Acetate