Clinical and Experimental Dermatology · 2005 · 12 citations · 8 references
Complement DepositionOcular DiseaseAutoimmune DiseaseOphthalmologyPathogenesisHistopathologyMucous Membrane PemphigoidCiliary BodyAutoimmunityAutoantibodiesOcular PathologyDermatologyMedicineOcular TissueMucous Membranes
Mucous membrane pemphigoid is a rare, chronic autoimmune disease characterized by subepidermal blistering and scarring, predominantly affecting mucous membranes. Ocular involvement frequently occurs and often represents the only manifestation of the disease. We describe a 62-year-old woman with a bilateral 18-month duration of conjunctival hyperaemia, associated with erythema and oedema of the eyelids, lacking any typical ocular signs of mucous membrane pemphigoid such as sub-conjuctival fibrosis and scarring. Histology was not significant. Direct immunofluorescence of the conjunctiva showed IgG, IgA and complement deposition along the basement membrane zone. Immunoprecipitation analysis of affinity purified laminin-5 revealed a band consistent with the beta3 chain of laminin-5. This represents the first case of pure ocular mucous membrane pemphigoid associated with anti-laminin-5 antibodies.
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Laminin 5 Binds the NC-1 Domain of Type VII Collagen
Patricia Rousselle, Douglas R. Keene, Florence Ruggiero et al. · The Journal of Cell Biology · 1997 · 252 citations · Full text