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Pemphigoid nodularis with IgA autoantibodies against the intracellular domain of desmoglein 1
Author(s) -
Fujisawa H.,
Ishii Y.,
Tateishi T.,
Kawachi Y.,
Otsuka F.,
Amagai M.,
Komai A.,
Hashimoto T.
Publication year - 2000
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1046/j.1365-2133.2000.03257.x
Subject(s) - desmoglein 1 , autoantibody , desmoglein 3 , pemphigus foliaceus , pemphigus vulgaris , antibody , bullous pemphigoid , medicine , immunology , desmoglein , antigen , pemphigus
Pemphigoid nodularis is a rare variant of bullous pemphigoid. We report a 49‐year‐old Japanese male with clinical and histopathological features of pemphigoid nodularis including circulating and in vivo ‐bound IgG antibasement membrane zone antibodies and IgA anti‐intercellular antibodies. Although the precise molecular target of the IgG autoantibodies could not be determined, intriguingly, immunoblotting showed that the IgA in the patient’s serum reacted with the intracellular domain of desmoglein 1, the target antigen in cases of pemphigus foliaceus. However, the IgA did not react with the extracellular domain of desmoglein 1 in sensitive enzyme‐linked immunosorbent assay studies using a baculovirus system. These results suggest therefore that these IgA antibodies may possibly not be pathogenic. The mechanism for the production of different autoantibodies is unknown, but this case provides further illustration of the atypical skin immunoreactants often seen in this unusual subtype of bullous pemphigoid.