Adoptive protection from experimental myasthenia gravis with T cells from mice treated nasally with acetylcholine receptor epitopes

J Neuroimmunol. 2002 Feb;123(1-2):123-34. doi: 10.1016/s0165-5728(01)00454-4.

Abstract

Nasal administration of synthetic CD4(+) epitopes of the acetylcholine receptor (AChR) prevents experimental myasthenia gravis (EMG) in C57Bl/6 mice, but not in IL4-deficient C57Bl/6 (IL4(-/-)) mice. Here we verify that nasal tolerance requires IL4, by showing that CD4(+) cells from C57Bl/6 mice treated nasally with a pool of AChR CD4(+) epitopes protected IL4(-/-) mice from EMG and caused a reduced production of anti-AChR antibody. CD4(+) cells from C57Bl/6 mice treated with unrelated peptides or sham-treated did not induce protection. CD4(+) cells from C57Bl/6 mice treated with just one AChR peptide protected IL4(-/-) mice from EMG without affecting antibody synthesis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Intranasal
  • Adoptive Transfer*
  • Animals
  • Antibodies / blood
  • CD4-Positive T-Lymphocytes / immunology*
  • Epitopes, T-Lymphocyte*
  • Female
  • Immunization
  • Immunoglobulin G / classification
  • Immunophenotyping
  • Interferon-gamma / biosynthesis
  • Interleukin-4 / biosynthesis
  • Mice
  • Myasthenia Gravis, Autoimmune, Experimental / prevention & control*
  • Receptors, Cholinergic / analysis
  • Receptors, Cholinergic / immunology*

Substances

  • Antibodies
  • Epitopes, T-Lymphocyte
  • Immunoglobulin G
  • Receptors, Cholinergic
  • Interleukin-4
  • Interferon-gamma