Suppression of experimental autoimmune myasthenia gravis by intravenous immunoglobulin and isolation of a disease-specific IgG fraction

Sara Fuchs, Tali Feferman, Kai Yun Zhu, Roberto Meidler, Raanan Margalit, Ningshan Wang, Orgad Laub, Miriam C. Souroujon

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

Intravenous immunoglobulin (IVIG) administration has been beneficially used for the treatment of a variety of autoimmune diseases including myasthenia gravis (MG). We have demonstrated that IVIG administration in experimental autoimmune MG (EAMG) results in suppression of disease that is accompanied by decreased Th1 cell and B cell proliferation. Chromatography of pooled human immunoglobulins (IVIGs) on immobilized IgG, isolated from rats with EAMG, results in a complete depletion of the suppressive activity of the IVIG. Moreover, the eluate from this EAMG-specific antibody column retains the immunosuppressive activity of IVIG. This study supports the notion that the therapeutic effect of IVIGs is mediated by an antigen-specific anti-immunoglobulin (anti-idiotypic) activity that is essential for its suppressive activity.

Original languageEnglish
Title of host publicationAutoimmunity, Part B Novel Applications of Basic Research
PublisherBlackwell Publishing Inc.
Pages550-558
Number of pages9
ISBN (Print)1573317098, 9781573317092
DOIs
StatePublished - Sep 2007

Publication series

NameAnnals of the New York Academy of Sciences
Volume1110
ISSN (Print)0077-8923
ISSN (Electronic)1749-6632

Keywords

  • Experimental autoimmune myasthenia gravis (EAMG)
  • Immunotherapy
  • Intravenous immunoglobulin (IVIG)
  • Myasthenia gravis (MG)

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