Autoimmunity to endoplasmic reticulum chaperone GRP94 in myasthenia gravis

J Neuroimmunol. 2011 Aug 15;237(1-2):87-92. doi: 10.1016/j.jneuroim.2011.06.011. Epub 2011 Jul 20.

Abstract

Immune responses to ER stress have been closely related to the pathogenesis of autoimmune diseases. Using an immunoprecipitation assay, 24 (7.1%) of 336 MG serum samples immunoprecipitated a 90-kDa protein from the muscle cellular extracts, but none of the disease or healthy control sera. The 90-kDa protein was affinity-purified and found to match to ER chaperon GRP94 by matrix-assisted laser desorption/ionization-time of flight mass spectroscopy analysis. The frequency of associated autoimmune diseases was much higher in the anti-GRP94-positive than the -negative patients (71% versus 11%, p<0.001). Autoimmunity to ER chaperone GRP94 is associated with a subset of MG patients who have additional autoimmune diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Autoantibodies / biosynthesis
  • Autoantibodies / blood
  • Autoantigens / biosynthesis
  • Autoantigens / blood
  • Cell Line, Tumor
  • Endoplasmic Reticulum / immunology*
  • Endoplasmic Reticulum / metabolism
  • Female
  • Humans
  • Male
  • Membrane Glycoproteins / immunology*
  • Middle Aged
  • Molecular Chaperones / immunology*
  • Myasthenia Gravis / immunology*
  • Myasthenia Gravis / metabolism*
  • Retrospective Studies
  • Young Adult

Substances

  • Autoantibodies
  • Autoantigens
  • Membrane Glycoproteins
  • Molecular Chaperones
  • endoplasmin