
pmid: 16635589
Pemphigus vulgaris (PV) is a potentially fatal autoimmune mucocutaneous disease associated with production of IgG autoantibodies to desmoglein 3 (Dsg3), a 130-kDa epidermal cadherin protein. The binding of pathogenic antibody to Dsg3 on epidermal keratinocytes leads to loss of intercellular adhesion and results in intraepithelial blister formation. Here, we describe a human monoclonal antibody, PVMAB786, a Dsg3-specific IgG4 antibody, from an untreated patient with active PV. The antibody reacts with a 130-kDa protein on keratinocyte cell surfaces and recombinant Dsg3 protein, but not desmoglein 1 protein. PVMAB786 induces acantholysis in normal human skin and mucous membranes and induces a clinical and histological profile similar to human PV when injected into neonatal mice. PVMAB786 will be a valuable tool in identifying the role of Dsg3 in epithelial cell adherence and acantholysis, mechanisms of Dsg3 processing/presentation and V gene and isotype usage in PV pathogenesis.
Keratinocytes, Mice, Inbred BALB C, Desmoglein 3, Blotting, Western, Antibodies, Monoclonal, Intradermal Tests, Immunohistochemistry, Mice, Acantholysis, Animals, Newborn, Immunoglobulin G, Animals, Humans, Immunotherapy, Fluorescent Antibody Technique, Indirect, Epitope Mapping, Pemphigus
Keratinocytes, Mice, Inbred BALB C, Desmoglein 3, Blotting, Western, Antibodies, Monoclonal, Intradermal Tests, Immunohistochemistry, Mice, Acantholysis, Animals, Newborn, Immunoglobulin G, Animals, Humans, Immunotherapy, Fluorescent Antibody Technique, Indirect, Epitope Mapping, Pemphigus
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