Pemphigoid diseases are a group of autoimmune vesiculobullous diseases, clinically characterized by tense blisters and erosions on the skin and/or mucous membranes. Mucous Membrane Pemphigoid (MMP), formerly referred to as cicatricial pemphigoid, is a subset of pemphigoid, affecting predominantly the mucosae [1]. MMP frequently involves the oral cavity [2], especially the gingiva [1–3]. Gingival manifestation of MMP is called Desquamative Gingivitis (DG), which is characterized by desquamation, erythema, erosions of the gingival epithelial, and vesiculobullous lesions [4,5]. The autoantigens of MMP that have been identified by circulating autoantibodies in the patients’ sera include 180 kDa bullous pemphigoid antigen 2 (BP180) [1,6–9] and bullous pemphigoid antigen 1 (BP230) [10–12], two hemidesmosome components.

Crossreactivity: The possible role of oral microbiota in oral mucous membrane pemphigoid

Lauritano D.
Ultimo
Supervision
2021

Abstract

Pemphigoid diseases are a group of autoimmune vesiculobullous diseases, clinically characterized by tense blisters and erosions on the skin and/or mucous membranes. Mucous Membrane Pemphigoid (MMP), formerly referred to as cicatricial pemphigoid, is a subset of pemphigoid, affecting predominantly the mucosae [1]. MMP frequently involves the oral cavity [2], especially the gingiva [1–3]. Gingival manifestation of MMP is called Desquamative Gingivitis (DG), which is characterized by desquamation, erythema, erosions of the gingival epithelial, and vesiculobullous lesions [4,5]. The autoantigens of MMP that have been identified by circulating autoantibodies in the patients’ sera include 180 kDa bullous pemphigoid antigen 2 (BP180) [1,6–9] and bullous pemphigoid antigen 1 (BP230) [10–12], two hemidesmosome components.
2021
Lucchese, A.; Petruzzi, M.; Lauritano, D.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2459824
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