Helicobacter pylori outer membrane vesicles inhibit human T cell responses via induction of monocyte COX-2 expression

Pathog Dis. 2017 Jun 1;75(4). doi: 10.1093/femspd/ftx034.

Abstract

The modulation of T cell responses by Helicobacter pylori is thought to potentiate both H. pylori persistence and development of gastric pathologies including cancer. Release of outer membrane vesicles (OMV) by H. pylori provides a potential vehicle for modulation of the immune system. Although OMV are thought to have T cell suppressive activity, this has not yet been demonstrated. Their suppressive activity was investigated in this study using the responses of peripheral blood mononuclear cells (PBMC) to T cell stimuli as a readout. We demonstrate that addition of OMV to PBMC significantly inhibits subsequent T cell proliferation in a cyclo-oxygenase-2 (COX-2)-dependent manner. Addition of OMV did not significantly modulate PBMC apoptosis, but induced strong expression of COX-2 by the monocytes present and significantly increased levels of PGE2 and IL-10. These effects were independent of vacuolating cytotoxin expression. Together, these findings demonstrate that OMV can suppress human T cell responses and that the predominant mechanism is not through a direct effect on the T cells but results from the induction of COX-2 expression in monocytes. This increased COX-2 activity may modulate not only H. pylori-directed immune responses but also wider immune responses.

Keywords: Helicobacter pylori; PGE2; T cell, COX-2; immune response; outer membrane vesicles.

MeSH terms

  • Cell-Derived Microparticles / metabolism*
  • Cells, Cultured
  • Cyclooxygenase 2 / metabolism*
  • Helicobacter pylori / immunology*
  • Host-Pathogen Interactions*
  • Humans
  • Immune Evasion
  • Immune Tolerance*
  • Monocytes / enzymology*
  • T-Lymphocytes / immunology*

Substances

  • Cyclooxygenase 2
  • PTGS2 protein, human