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大疱性类天疱疮中的IgA基底膜带自身抗体通过免疫印迹法检测分子量为270 - 280 kDa、230 kDa和180 kDa的表皮抗原。

IgA basement membrane zone autoantibodies in bullous pemphigoid detect epidermal antigens of 270-280 kDa, 230 kDa, and 180 kDa molecular weight by immunoblotting.

作者信息

Kirtschig G, Wojnarowska F

机构信息

Department of Dermatology, Churchill Hospital, Oxford, UK.

出版信息

Clin Exp Dermatol. 1999 Jul;24(4):302-7. doi: 10.1046/j.1365-2230.1999.00485.x.

DOI:10.1046/j.1365-2230.1999.00485.x
PMID:10457136
Abstract

Bullous pemphigoid (BP) is an acquired subepidermal blistering disease characterized by circulating IgG autoantibodies binding to the 230 and 180 kDa hemidesmosomal proteins. Associated basement membrane zone (BMZ) autoantibodies of the IgA class have been reported in few BP patients. The incidence and clinical relevance of these IgA antibodies, as well as their target antigens are unknown. Sera of 26 patients with BP were analysed for circulating IgG- and IgA-anti-BMZ autoantibodies by indirect immunofluorescence on salt-split human skin. All of the patients had circulating IgG autoantibodies and, in addition, nine (35%) also had circulating anti-BMZ IgA antibodies, that bound to the epidermal side of salt-split skin. By immunoblotting, IgA antibodies in seven of nine sera recognized either the 180 kDa, the 230 kDa, or both BP antigens. Moreover, IgA anti-BMZ antibodies in seven sera also detected an epidermal protein of 270-280 kDa. IgA antibodies did not identify specific bands on immunoblots of dermal extracts. There was no clinical difference between BP patients with or without circulating anti-BMZ-IgA.

摘要

大疱性类天疱疮(BP)是一种获得性表皮下疱病,其特征为循环中的IgG自身抗体与230kDa和180kDa的半桥粒蛋白结合。少数BP患者中曾报道有相关的IgA类基底膜带(BMZ)自身抗体。这些IgA抗体的发生率、临床相关性及其靶抗原均未知。通过对盐裂人皮肤进行间接免疫荧光分析,检测了26例BP患者血清中的循环IgG和IgA抗BMZ自身抗体。所有患者均有循环IgG自身抗体,此外,9例(35%)还具有循环抗BMZ IgA抗体,其与盐裂皮肤的表皮侧结合。通过免疫印迹法,9份血清中的7份血清中的IgA抗体识别了180kDa、230kDa或两种BP抗原。此外,7份血清中的IgA抗BMZ抗体还检测到一种270 - 280kDa的表皮蛋白。IgA抗体在真皮提取物的免疫印迹上未识别出特异性条带。有或无循环抗BMZ-IgA的BP患者之间无临床差异。

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