Complement-independent blistering mechanisms in bullous pemphigoid

被引:23
作者
Iwata, Hiroaki [1 ]
Ujiie, Hideyuki [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Dermatol, Sapporo, Hokkaido, Japan
关键词
bullous pemphigoid; collagen XVII; complement; XVII COLLAGEN; MOUSE MODEL; DIRECT IMMUNOFLUORESCENCE; ALPHA(6)BETA(4) INTEGRIN; IGG4; AUTOANTIBODIES; AUTOIMMUNE-DISEASE; BASEMENT-MEMBRANE; ANTIGEN; BP180; ANTIBODY;
D O I
10.1111/exd.13367
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Bullous pemphigoid (BP) is an autoimmune subepidermal blistering disease that clinically demonstrates tense blisters with widespread erythema, histologically demonstrates subepidermal blistering and immunologically demonstrates the presence of circulating autoantibodies against hemidesmosomal molecules. Complement activation has long been regarded as necessary for the generation of the BP, However, certain evidence has recently come to support non-complemental blistering mechanisms. The story of BP blistering mechanisms is a complicated one. This review mainly focuses on a specific blistering mechanism that highlights the role of complements in BP blistering.
引用
收藏
页码:1235 / 1239
页数:5
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