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Mechanisms of acantholysis in pemphigus vulgaris: role of IgG valence.

Abstract
Pemphigus vulgaris (PV) is a dermatosis mediated by autoantibodies against desmoglein 3 (Dsg3). It was known that intraperitoneal (i.p.) injections of PV IgG and PV F(ab')2, but not of PV Fab, into neonatal mice reproduced the key features of the disease in these animals. It was proposed that crosslinking of antigen by bivalent PV autoantibodies may trigger acantholysis in PV. In the present study, we have used subcutaneous (s.c.) injections of PV IgG and its proteolytic fragments into neonatal mice to test equimolar amounts of these autoantibody fractions. Mice developed clinical and histological features of PV in a dose-dependent manner following a similar time course. PV IgG and Fab fractions induced acantholysis as early as 2 hr after the injection. It was also demonstrated that sc injections of PV Fab were more effective in inducing disease than ip injections. PV autoantibodies may bind an "adhesive site" of Dsg3 and impair its function, thus triggering acantholysis.
AuthorsJ M Mascaró Jr, A España, Z Liu, X Ding, S J Swartz, J A Fairley, L A Diaz
JournalClinical immunology and immunopathology (Clin Immunol Immunopathol) Vol. 85 Issue 1 Pg. 90-6 (Oct 1997) ISSN: 0090-1229 [Print] United States
PMID9325074 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Autoantibodies
  • Cadherins
  • DSG3 protein, human
  • Desmoglein 3
  • Immunoglobulin Fab Fragments
  • Immunoglobulin G
Topics
  • Acantholysis (etiology, immunology, pathology)
  • Animals
  • Animals, Newborn
  • Antigen-Antibody Reactions
  • Autoantibodies (administration & dosage, blood, chemistry)
  • Binding Sites
  • Cadherins (immunology)
  • Desmoglein 3
  • Humans
  • Immunization, Passive
  • Immunoglobulin Fab Fragments (administration & dosage, blood, chemistry)
  • Immunoglobulin G (administration & dosage, blood, chemistry)
  • Injections, Subcutaneous
  • Mice
  • Mice, Inbred BALB C
  • Pemphigus (complications, immunology, pathology)

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