Classification and Antigen Molecules of Autoimmune Bullous Diseases

被引:6
作者
Hashimoto, Takashi [1 ]
Qian, Hua [2 ]
Ishii, Norito [3 ]
Nakama, Takekuni [3 ]
Tateishi, Chiharu [1 ]
Tsuruta, Daisuke [1 ]
Li, Xiaoguang [2 ]
机构
[1] Osaka Metropolitan Univ Grad Sch Med, Dept Dermatol, Osaka 5458585, Japan
[2] Dalian Univ, Med Coll, Dept Lab Med, Dalian 116622, Peoples R China
[3] Kurume Univ, Sch Med, Dept Dermatol, Kurume 8300011, Japan
基金
日本学术振兴会;
关键词
autoimmune bullous diseases; autoantibody; classification; autoantigen molecules; subtypes; pemphigus; pemphigoid; nomenclature; C-TERMINAL DOMAIN; IGE AUTOANTIBODIES; IMMUNOLOGICAL PROFILES; JAPANESE PATIENTS; MOUSE MODEL; PEMPHIGUS; BP180; COEXISTENCE; PSORIASIS; EPITOPE;
D O I
10.3390/biom13040703
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autoimmune bullous diseases (AIBDs), which are a group of tissue-specific autoimmune diseases of the skin, present with various blistering lesions on the skin and mucous membranes, and show autoantibodies of IgG, IgA and IgM against epidermal cell surfaces and basement membrane zone. To date, AIBDs have been classified into a number of distinct subtypes by clinical and histopathological findings, and immunological characteristics. In addition, various biochemical and molecular biological studies have identified various novel autoantigens in AIBDs, which has resulted in proposals of new subtypes of AIBDs. In this article, we summarized various distinct AIBDs, and proposed the latest and most comprehensive classification of AIBDs with their autoantigen molecules.
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页数:12
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