Autoimmune human T lymphocytes specific for acetylcholine receptor

Nature. 1984 Jul;310(5974):244-6. doi: 10.1038/310244a0.

Abstract

Myasthenia gravis is one of the best characterized human autoimmune disorders. Circulating autoantibodies to the nicotinic acetylcholine receptor (AChR) at the neuromuscular junction play a prominent part in the effector phase, that is, the immunoregulation. Indirect evidence, such as thymic abnormalities and the association with certain histocompatibility antigens (for example HLA-B8,-DR3) suggests a defect of immunoregulation at the level of thymus-dependent (T) lymphocytes. We report here on the isolation of autoreactive T cells from six patients with myasthenia gravis. From one of these patients, who is homozygous for HLA-DR3, we established a long-term T-cell line. The line cells are specific for purified fish and human AChR, display the surface phenotype of inducer/helper T cells and are genetically restricted to HLA-DR3. AChR-induced proliferation could be inhibited with two monoclonal antibodies against monomorphic DR determinants and also with DR3-specific alloantiserum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoimmune Diseases / immunology*
  • Cell Line
  • Cell Separation
  • HLA-DR Antigens
  • HLA-DR3 Antigen
  • Histocompatibility Antigens Class II / analysis
  • Histocompatibility Antigens Class II / immunology
  • Humans
  • Myasthenia Gravis / genetics
  • Myasthenia Gravis / immunology*
  • Phenotype
  • Receptors, Cholinergic / immunology*
  • T-Lymphocytes / immunology*

Substances

  • HLA-DR Antigens
  • HLA-DR3 Antigen
  • Histocompatibility Antigens Class II
  • Receptors, Cholinergic