Intracellular bacteria can cause EAE in SJL mice or modify self-specific T cell repertoire

J Neurol Sci. 2011 Dec 15;311(1-2):103-6. doi: 10.1016/j.jns.2011.08.042. Epub 2011 Sep 13.

Abstract

Environment and genetic are both relevant in determining development of Multiple Sclerosis. Many epidemiological observations converge on indicating EBV infection and Vitamin D levels as major players among the environmental factors. Bacteria and bacterial products are however potent triggers of immune responses, and recent work from several laboratories indicates that the microbiota plays a prominent role in "priming" or protecting individuals for development of experimental autoimmune diseases. Here we report our recent work dealing with the role of non-pathogenic mycobacteria and their innate receptors in relapsing-remitting experimental autoimmune encephalomyelitis in the SJL mouse and in mobilization of CNS-reactive T cells. We finally discuss how bacteria are likely involved in the pathogenesis of Multiple Sclerosis, expecially with regard to their role in driving the recurring acute episodes of disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Encephalomyelitis, Autoimmune, Experimental / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / microbiology*
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Epitopes, T-Lymphocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism*
  • Intracellular Space / immunology
  • Intracellular Space / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Multiple Sclerosis, Relapsing-Remitting / immunology*
  • Multiple Sclerosis, Relapsing-Remitting / microbiology*
  • Multiple Sclerosis, Relapsing-Remitting / pathology
  • Mycobacterium tuberculosis / immunology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / microbiology*
  • T-Lymphocyte Subsets / pathology
  • Tuberculosis / immunology
  • Tuberculosis / microbiology
  • Tuberculosis / pathology

Substances

  • Epitopes, T-Lymphocyte