Yang Miao, Wu Haijing, Zhao Ming, Chang Christopher, Lu Qianjin
Department of Dermatology, Hunan Key Laboratory of Medical Epigenomics, The second Xiangya Hospital of Central South University, Changsha, Hunan, 410011, PR China.
Division of Rheumatology, Allergy and Clinical Immunology, University of California, Davis, CA, 95616, USA.
J Transl Autoimmun. 2019 Aug 26;2:100014. doi: 10.1016/j.jtauto.2019.100014. eCollection 2019 Dec.
Bullous skin diseases are a group of dermatoses characterized by blisters and bullae in the skin and mucous membranes. The etiology and pathogenesis of bullous skin diseases are not completely clear. The most common are pemphigus and bullous pemphigoid (BP). Autoantibodies play critical roles in their pathogenesis. Abnormalities in the adhesion between keratinocytes in patients with pemphigus leads to acantholysis and formation of intra-epidermal blisters. Anti-desmoglein autoantibodies are present both in the circulation and skin lesions of patients with pemphigus. The deficient adhesion of keratinocytes to the basement membrane in BP patients gives rise to subepidermal blisters. Autoantibodies against the components of hemidesmosome can be detected in BP patients. Many novel therapeutics based on knowledge of the pathogenesis have emerged in recent years.
大疱性皮肤病是一组以皮肤和黏膜出现水疱和大疱为特征的皮肤病。大疱性皮肤病的病因和发病机制尚未完全明确。最常见的是天疱疮和大疱性类天疱疮(BP)。自身抗体在其发病机制中起关键作用。天疱疮患者角质形成细胞间黏附异常导致棘层松解和表皮内水疱形成。抗桥粒芯糖蛋白自身抗体存在于天疱疮患者的循环系统和皮肤损害中。BP患者角质形成细胞与基底膜的黏附缺陷导致表皮下水疱形成。在BP患者中可检测到针对半桥粒成分的自身抗体。近年来,基于发病机制的认识出现了许多新型治疗方法。