Experimental autoimmune encephalomyelitis development is aggravated by Candida albicans infection

J Immunol Res. 2015:2015:635052. doi: 10.1155/2015/635052. Epub 2015 Apr 19.

Abstract

Multiple sclerosis (MS) is an inflammatory/autoimmune disease of the central nervous system (CNS) mainly mediated by myelin specific T cells. It is widely believed that environmental factors, including fungal infections, contribute to disease induction or evolution. Even though Candida infection among MS patients has been described, the participation of this fungus in this pathology is not clear. The purpose of this work was to evaluate the effect of a Candida albicans infection on experimental autoimmune encephalomyelitis (EAE) that is a widely accepted model to study MS. Female C57BL/6 mice were infected with C. albicans and 3 days later, animals were submitted to EAE induction by immunization with myelin oligodendrocyte glycoprotein. Previous infection increased the clinical score and also the body weight loss. EAE aggravation was associated with expansion of peripheral CD4(+) T cells and production of high levels of TNF-α, IFN-γ IL-6, and IL-17 by spleen and CNS cells. In addition to yeast and hyphae, fungus specific T cells were found in the CNS. These findings suggest that C. albicans infection before EAE induction aggravates EAE, and possibly MS, mainly by CNS dissemination and local induction of encephalitogenic cytokines. Peripheral production of encephalitogenic cytokines could also contribute to disease aggravation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • Candida albicans / immunology
  • Candidiasis / immunology*
  • Cells, Cultured
  • Central Nervous System / cytology
  • Central Nervous System / immunology*
  • Central Nervous System / microbiology*
  • Disease Models, Animal
  • Encephalomyelitis, Autoimmune, Experimental / immunology*
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Female
  • Interferon-gamma / metabolism
  • Interleukin-17 / metabolism
  • Interleukin-6 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / pathology
  • Myelin-Oligodendrocyte Glycoprotein / pharmacology
  • Peptide Fragments / pharmacology
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Il17a protein, mouse
  • Interleukin-17
  • Interleukin-6
  • Myelin-Oligodendrocyte Glycoprotein
  • Peptide Fragments
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma