Suppression of experimental allergic encephalomyelitis by intraventricular administration of interferon-gamma in Lewis rats

Clin Exp Immunol. 1990 Aug;81(2):183-8. doi: 10.1111/j.1365-2249.1990.tb03315.x.

Abstract

Experimental allergic encephalomyelitis (EAE) is an autoimmune inflammatory disease of the central nervous system (CNS) which causes paralysis. Several studies have reported the involvement of Ia antigen-expressing cells in the pathogenesis of EAE. Interferon-gamma (IFN-gamma) can induce Ia antigen expression on a wide range of cells. We examined the effect of IFN-gamma on EAE in Lewis rats. Systemically administered IFN-gamma did not change the disease course of EAE, whereas IFN-gamma applied locally into the ventricular system of the CNS resulted in complete suppression of clinical signs. Furthermore, we found that systemic administration of anti-IFN-gamma just prior to the onset of clinical symptoms resulted in a more severe disease course. We conclude that IFN-gamma is capable of exerting a suppressive action in EAE, possibly through induction of Ia antigen expression or through the induction of suppressive mechanisms locally in the CNS.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / therapeutic use
  • Cerebellum / immunology
  • Cerebellum / pathology
  • Encephalomyelitis, Autoimmune, Experimental / pathology
  • Encephalomyelitis, Autoimmune, Experimental / prevention & control*
  • Encephalomyelitis, Autoimmune, Experimental / therapy
  • Histocompatibility Antigens Class II / biosynthesis
  • Immunoenzyme Techniques
  • Injections, Intraperitoneal
  • Injections, Intraventricular
  • Interferon-gamma / administration & dosage
  • Interferon-gamma / immunology
  • Interferon-gamma / therapeutic use*
  • Male
  • Optic Nerve / immunology
  • Optic Nerve / pathology
  • Rats
  • Rats, Inbred Lew
  • Recombinant Proteins

Substances

  • Antibodies, Monoclonal
  • Histocompatibility Antigens Class II
  • Recombinant Proteins
  • Interferon-gamma