Demonstration of strong enterobacterial reactivity of CD4+CD25- T cells from conventional and germ-free mice which is counter-regulated by CD4+CD25+ T cells

Eur J Immunol. 2004 Mar;34(3):695-704. doi: 10.1002/eji.200324394.

Abstract

Unfractionated CD4+ T cells from the gut-associated lymphoid tissue (GALT) and peripheral lymph nodes are unresponsive when exposed to enterobacterial antigens in vitro. Under similar conditions, CD4+ T cells depleted in vivo or in vitro of CD4+CD25+ T cells proliferate extensively. The CD4+CD25- T cell reactivity depends on MHC class II presentation, specific TCR stimulation, CD4 ligation, and antigen processing by antigen-presenting cells. The CD4+CD25- T cells respond to autologous and heterologous enterobacterial antigens, but not to antigens from the feces of germ-free mice. Surprisingly, CD4+CD25- T cells obtained from the GALT of germ-free mice also proliferate when exposed to enterobacterial antigens, and adding back the conventional or germ-free CD4+CD25+ T cells to the enteroantigen-stimulated CD4+CD25- T cells abolishes proliferation. As judged from carboxyfluorescein diacetate succinimidyl ester-labeling experiments, 4-5% of the CD4+CD25- T cells respond to enteroantigen. The data show for the first time that CD4+CD25- T cells with reactivity towards the enterobacterial flora and regulatory CD4+CD25- T cells are present in both conventional and germ-free mice. The data suggest that a significant proportion of the peripheral pool of CD4+CD25- T cells express anti-enterobacterial reactivity, which, due to the presence of regulatory CD4+CD25+ T cells, is kept in a quiescent state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, Bacterial / immunology*
  • CD4-Positive T-Lymphocytes / classification
  • CD4-Positive T-Lymphocytes / immunology*
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Female
  • Histocompatibility Antigens Class II / metabolism
  • Immune Tolerance
  • Intestinal Mucosa / immunology*
  • Lymphocyte Activation*
  • Lymphocyte Depletion
  • Mice
  • Mice, Inbred BALB C
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Interleukin-2 / analysis*
  • Specific Pathogen-Free Organisms
  • T-Lymphocyte Subsets / immunology*
  • Th2 Cells / immunology

Substances

  • Antigens, Bacterial
  • Cytokines
  • Histocompatibility Antigens Class II
  • Receptors, Antigen, T-Cell
  • Receptors, Interleukin-2