FK506 prevents induction of rat experimental autoimmune myasthenia gravis

J Autoimmun. 1997 Feb;10(1):11-6. doi: 10.1006/jaut.1996.0111.

Abstract

Myasthenia gravis (MG) is an organ-specific autoimmune disease attacking nicotinic acetylcholine receptors (AChR) of the neuromuscular junction. Autoantibody production is regulated by autoimmune helper T cells that are specific to AChR. Therefore the suppression of autoimmune T cell activity could reduce myasthenic symptoms. Amongst immunomodulatory therapies aimed at T cells, we studied the therapeutic effect of FK506 as a T cell-specific immunosuppressive agent. Rats in which experimental autoimmune myasthenia gravis (EAMG) was induced by immunization with synthetic peptide of human AChR alpha-subunit residues 125-147 (H alpha 125-147) were treated daily with FK506 (1 mg/kg). FK506 prevented the reduction in amplitude of miniature endplate potential (MEPP) which was induced by H alpha 125-147 immunization. FK506 also suppressed anti-H alpha 125-147 and anti-rat AChR antibody production accompanied by a decrease in the antigen-specific T cell response against H alpha 125-147. These findings indicate that FK506 prevents induction of rat EAMG evoked by immunizing T cells against H alpha 125-147.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies / analysis
  • Cell Division
  • Disease Models, Animal
  • Electrophysiology
  • Female
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Molecular Sequence Data
  • Myasthenia Gravis / prevention & control*
  • Peptide Fragments / immunology
  • Rats
  • Rats, Inbred Lew
  • Receptors, Nicotinic / immunology*
  • Tacrolimus / therapeutic use*

Substances

  • Antibodies
  • Immunosuppressive Agents
  • Peptide Fragments
  • Receptors, Nicotinic
  • Tacrolimus