Helicobacter pylori has stimulatory effects on naive T cells

Helicobacter. 2006 Feb;11(1):21-30. doi: 10.1111/j.0083-8703.2006.00374.x.

Abstract

Background: Despite an apparently active host response, Helicobacter pylori infection can persist for life. Unexpectedly, T cells from apparently uninfected individuals respond to H. pylori antigen by proliferating. Also, the T-cell proliferative response appears to be less in infected compared with uninfected individuals.

Materials and methods: We have investigated the T-cell response of isolated human peripheral blood, naive, and memory CD4+ T cells to H. pylori antigen in infected and uninfected subjects.

Results: In agreement with previous findings, the peripheral blood proliferative response was higher in uninfected compared with infected subjects. Interestingly, there was a response in CD4+ CD45RO+ (memory) and CD4+CD45RA+ (naive) subsets. The RO/RA ratio of the response to H. pylori antigen was 0.8-2.1 in both H. pylori-positive and H. pylori-negative subjects, which was similar to that of a known superantigen (2.5 and 2.2 in Helicobacter-positive and -negative subjects, respectively) whereas the RO/RA response ratio to a recall antigen (tetanus toxoid) was 9.8 and 18.7 in Helicobacter-positive and -negative subjects, respectively. Mononuclear cells isolated from cord blood also responded to H. pylori antigen, whereas there was no response to tetanus toxoid. The cord blood response and CD4+ CD45RA+ cell response to H. pylori antigen were inhibited predominantly by anti-HLA-DR and to some extent by anti-HLA-DQ antibodies. Investigation of the response to five different recombinant H. pylori antigens identified two that produced a response in naive T cells.

Conclusions: These data suggest that H. pylori possesses molecules that cause higher than expected proliferation of naive T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antigens, Bacterial / genetics
  • Antigens, Bacterial / pharmacology
  • Bacterial Proteins / genetics
  • Bacterial Proteins / pharmacology
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / microbiology
  • Cell Proliferation
  • Cells, Cultured
  • HLA-DP Antigens / immunology
  • HLA-DQ Antigens / immunology
  • HLA-DR Antigens / immunology
  • Helicobacter pylori / pathogenicity*
  • Humans
  • Immunologic Memory*
  • Leukocyte Common Antigens / immunology
  • Recombinant Proteins / pharmacology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / microbiology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Bacterial
  • Bacterial Proteins
  • HLA-DP Antigens
  • HLA-DQ Antigens
  • HLA-DR Antigens
  • Recombinant Proteins
  • cagA protein, Helicobacter pylori
  • Leukocyte Common Antigens