Zillikens D, Caux F, Mascaro J M, Wesselmann U, Schmidt E, Prost C, Callen J P, Bröcker E B, Diaz L A, Giudice G J
Department of Dermatology, University of Würzburg, Germany.
J Invest Dermatol. 1999 Jul;113(1):117-21. doi: 10.1046/j.1523-1747.1999.00618.x.
Lichen planus pemphigoides is an autoimmune subepidermal blistering disease. The finding of immunoglobulin G antibodies directed against the basement membrane zone differentiates it from bullous lichen planus. The aim of this study was to identify the target antigen of lichen planus pemphigoides autoantibodies. Sera from lichen planus pemphigoides patients (n = 4) stained the epidermal side of NaCl-split human skin in a pattern indistinguishable from that produced by bullous pemphigoid sera. In bullous pemphigoid, the autoimmune response is directed against BP180, a hemidesmosomal transmembrane collagenous glycoprotein. We previously demonstrated that bullous pemphigoid sera predominantly react with a set of four epitopes (MCW-0 through MCW-3) clustered within a 45 amino acid stretch of the major noncollagenous extracellular domain (NC16A) of BP180. By immunoblotting and enzyme-linked immunosorbent assay, lichen planus pemphigoides sera were also strongly reactive with recombinant bullous pemphigoid 180 NC16A. The lichen planus pemphigoides epitopes were further mapped using a series of overlapping recombinant segments of the NC16A domain. All lichen planus pemphigoides sera reacted with amino acids 46-59 of domain NC16A, a protein segment that was previously shown to be unreactive with bullous pemphigoid sera. Two lichen planus pemphigoides sera, in addition, reacted with the immunodominant antigenic region associated with bullous pemphigoid. In conclusion, there are now five bullous diseases that are associated with an autoimmune response to BP180: bullous pemphigoid; pemphigoid/herpes gestationis; cicatricial pemphigoid; linear immunoglobulin A disease; and lichen planus pemphigoides. In addition, we have identified a novel epitope within the BP180 NC16A domain, designated MCW-4, that appears to be uniquely recognized by sera from patients with lichen planus pemphigoides.
扁平苔藓类天疱疮是一种自身免疫性表皮下大疱性疾病。针对基底膜带的免疫球蛋白G抗体的发现使其与大疱性扁平苔藓相鉴别。本研究的目的是鉴定扁平苔藓类天疱疮自身抗体的靶抗原。扁平苔藓类天疱疮患者(n = 4)的血清以与大疱性类天疱疮血清产生的模式无法区分的方式染色NaCl分离的人皮肤的表皮侧。在大疱性类天疱疮中,自身免疫反应针对BP180,一种半桥粒跨膜胶原糖蛋白。我们先前证明大疱性类天疱疮血清主要与BP180主要非胶原细胞外结构域(NC16A)的45个氨基酸片段内聚集的一组四个表位(MCW-0至MCW-3)反应。通过免疫印迹和酶联免疫吸附测定,扁平苔藓类天疱疮血清也与重组大疱性类天疱疮180 NC16A强烈反应。使用NC16A结构域的一系列重叠重组片段进一步定位扁平苔藓类天疱疮表位。所有扁平苔藓类天疱疮血清均与NC16A结构域的氨基酸46-59反应,该蛋白片段先前显示与大疱性类天疱疮血清无反应。此外,两份扁平苔藓类天疱疮血清还与与大疱性类天疱疮相关的免疫显性抗原区域反应。总之,现在有五种大疱性疾病与针对BP180的自身免疫反应相关:大疱性类天疱疮;类天疱疮/妊娠疱疹;瘢痕性类天疱疮;线状免疫球蛋白A病;和扁平苔藓类天疱疮。此外,我们在BP180 NC16A结构域内鉴定了一个新的表位,命名为MCW-4,它似乎是扁平苔藓类天疱疮患者血清唯一识别的。