Gastritis in urease-immunized mice after Helicobacter felis challenge may be due to residual bacteria

Gastroenterology. 1997 Oct;113(4):1118-28. doi: 10.1053/gast.1997.v113.pm9322506.

Abstract

Background & aims: Oral immunization with recombinant Helicobacter pylori urease (rUre) coadministered with a mucosal adjuvant protects mice against challenge with Helicobacter felis. In this study, the duration of protection and gastritis after challenge were characterized at sequential time intervals up to 1 year.

Methods: Outbred Swiss-Webster mice were orally immunized with rUre plus adjuvant and examined for the presence of H. felis infection and leukocyte infiltration into the gastric mucosa.

Results: When defined by gastric urease activity, 70%-95% of rUre-immunized mice were protected for between 2 and 57 weeks. Challenge with H. felis increased the inflammatory response in the gastric mucosa of rUre-immunized mice, which also had elevated CD4+ and CD8+ T cells. The CD8+ cells represented a population of gastric intraepithelial cells, which expressed the mucosal alpha E-integrin. Epithelial changes consisting of parietal cell loss and hyperplasia of the epithelium occurred in approximately 20% of the mice. Antimicrobial triple therapy significantly decreased the degree of gastritis and epithelial alteration in the stomach.

Conclusions: These results indicate that oral immunization of mice with rUre produces a long-lasting inhibition of H. felis infection but that residual bacteria may produce a persistent lymphocytic infiltration under these experimental conditions.

MeSH terms

  • Animals
  • Bacterial Vaccines*
  • Female
  • Flow Cytometry
  • Gastric Mucosa / immunology*
  • Gastric Mucosa / microbiology
  • Gastric Mucosa / pathology
  • Gastritis / microbiology*
  • Helicobacter / enzymology
  • Helicobacter / isolation & purification*
  • Helicobacter Infections / complications
  • Helicobacter Infections / immunology*
  • Helicobacter pylori / enzymology
  • Helicobacter pylori / immunology*
  • Immunophenotyping
  • Integrins / biosynthesis
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / microbiology
  • Intestinal Mucosa / pathology
  • Metaplasia
  • Mice
  • Receptors, Antigen, T-Cell, alpha-beta / biosynthesis
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / pathology
  • Urease / analysis
  • Urease / immunology*
  • Vaccines, Synthetic*

Substances

  • Bacterial Vaccines
  • Integrins
  • Receptors, Antigen, T-Cell, alpha-beta
  • Vaccines, Synthetic
  • Urease