Presynaptic membrane receptor-reactive T lymphocytes in myasthenia gravis

Scand J Immunol. 1996 Jan;43(1):81-7. doi: 10.1046/j.1365-3083.1996.d01-1.x.

Abstract

The majority of patients with myasthenia gravis were shown to have T and B cells specific for a beta-bungarotoxin binding protein, presynaptic membrane receptor (PsmR). Such autoreactive T cells may be subdivided into different subsets according to the pattern of cytokine production. In this study the authors examined the subpopulation of the T cells by analysing their IFN-gamma and/or IL-4 secretion pattern. T cell response to human muscle acetylcholine receptor (AChR) was examined in parallel. PsmR-stimulated IFN-gamma secretion was found in 60%, and IL-4 secretion in 48% of the patients. Cells stimulated to secrete both IFN-gamma and IL-4 or IFN-gamma only were the most common patterns. Treatment of the cells with a mouse anti-human HLA-DR antibody abolished the secretion of cytokines. There was a positive correlation between the numbers of PsmR-reactive and AChR-reactive T cells. In conclusion, the results show that PsmR-stimulated T cells secreted IFN-gamma and/or IL-4. This T cell response is MHC class II restricted. Thus, this study indicates that both Th1/Th2 or Th0 subsets of the T cells are involved in the autoimmune response in the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Bungarotoxins / metabolism
  • Female
  • HLA-DR Antigens / immunology
  • Humans
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / biosynthesis
  • Interleukin-4 / antagonists & inhibitors
  • Interleukin-4 / biosynthesis
  • Lymphocyte Activation / drug effects
  • Male
  • Mice
  • Middle Aged
  • Myasthenia Gravis / immunology*
  • Myasthenia Gravis / metabolism
  • Presynaptic Terminals / immunology
  • Receptors, Cholinergic / metabolism
  • Receptors, Presynaptic / metabolism*
  • Synaptic Membranes / immunology
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism*

Substances

  • Antibodies, Monoclonal
  • Bungarotoxins
  • HLA-DR Antigens
  • Receptors, Cholinergic
  • Receptors, Presynaptic
  • Interleukin-4
  • Interferon-gamma