Usefulness of immunofluorescence overlay antigen mapping in the identification of autoantigen in anti-p200 pemphigoid

J Dermatol. 2023 Sep;50(9):1194-1198. doi: 10.1111/1346-8138.16810. Epub 2023 Apr 20.

Abstract

Anti-p200 pemphigoid is a rare subepidermal blistering disease showing immunoglobulin G (IgG) autoantibodies reactive with a 200-kDa protein. In most patients, serum IgG antibodies react with laminin γ1. The diagnosis of anti-p200 pemphigoid is occasionally difficult, mainly due to the lack of standardized tests. We performed fluorescence overlay antigen mapping by laser scanning confocal microscopy (FOAM-LSCM) to identify autoantigens in an anti-p200 pemphigoid patient and assessed its usefulness for the diagnosis. A 71-year-old man presented with blisters and erosions on the bilateral forearms. No mucosal lesions were observed. Laboratory examinations revealed mild leukocytosis and antinuclear antibody negativity. A histopathological examination showed subepidermal blisters with neutrophil infiltration. Direct immunofluorescence showed linear IgG staining along the basement membrane zone. Indirect immunofluorescence using 1 M NaCl-split skin sections revealed IgG reactivity on the dermal side. Immunoblotting detected circulating IgG autoantibodies that reacted with a 200-kDa protein. Accordingly, anti-p200 pemphigoid was diagnosed. FOAM-LSCM revealed that the patient's IgG signals were co-localized with laminin γ1 but were observed above type VII collagens. A direct immunofluorescent analysis for IgG deposition patterns showed an n-serrated pattern. Thus, FOAM-LSCM may be useful for diagnosing anti-p200 pemphigoid.

Keywords: anti-p200 pemphigoid; autoantibodies; fluorescence overlay antigen mapping; laminin γ1; laser scanning confocal microscopy.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Autoantibodies
  • Autoantigens*
  • Blister / pathology
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Immunoglobulin G
  • Male
  • Pemphigoid, Bullous*

Substances

  • Autoantigens
  • Autoantibodies
  • Immunoglobulin G