Domloge-Hultsch N, Anhalt G J, Gammon W R, Lazarova Z, Briggaman R, Welch M, Jabs D A, Huff C, Yancey K B
Department of Dermatology, Uniformed Services University of the Health Sciences, Bethesda, Md.
Arch Dermatol. 1994 Dec;130(12):1521-9.
Epiligrin is a glycoprotein complex deposited in extracellular matrix by cultured human keratinocytes that serves as the major integrin ligand of these cells. In human skin, epiligrin is found at the interface of the lamina lucida and lamina densa in epidermal basement membrane where it is believed to be associated with anchoring filaments and plays an important role in keratinocyte adhesion.
We have identified six patients with a subepithelial bullous disorder of mucous membranes and skin who have IgG anti-basement membrane autoantibodies that immunoprecipitate epiligrin from human keratinocyte extracts and culture media. These patients' IgG autoantibodies also bind epiligrin in human keratinocyte extracellular matrix and epidermal basement membrane as determined by immunofluorescence and immunoelectron microscopy. Studies of 10 patients who are clinically indistinguishable from subjects with anti-epiligrin autoantibodies (ie, cicatricial pemphigoid patients) found that while seven had anti-basement membrane autoantibodies, the latter are directed exclusively against a region of epidermal basement membrane that does not contain epiligrin, are present in low titer (ie, < or = 1:10), do not react with keratinocyte extracellular matrix, and do not bind epiligrin (or any other specific antigen) in immunoprecipitation studies of human keratinocyte extracts or media. Antiepiligrin autoantibodies were also not detected in studies of 36 additional patients with bullous diseases or six normal volunteers.
Cicatricial pemphigoid is a disease phenotype in which patients' autoantibodies may target different constituents of epidermal basement membrane. Antiepiligrin autoantibodies are a specific immunologic marker for a group of patients with a disease entity that we propose to designate antiepiligrin cicatricial pemphigoid.
表皮整联配体蛋白是一种糖蛋白复合物,由培养的人角质形成细胞沉积于细胞外基质中,是这些细胞的主要整合素配体。在人皮肤中,表皮整联配体蛋白存在于表皮基底膜透明层和致密层的界面处,据信它与锚定细丝相关,并在角质形成细胞黏附中起重要作用。
我们鉴定出6例患有黏膜和皮肤上皮下大疱性疾病的患者,他们的IgG抗基底膜自身抗体可从人角质形成细胞提取物和培养基中免疫沉淀表皮整联配体蛋白。通过免疫荧光和免疫电子显微镜检测发现,这些患者的IgG自身抗体也与人角质形成细胞外基质和表皮基底膜中的表皮整联配体蛋白结合。对10例临床上与抗表皮整联配体蛋白自身抗体患者无法区分的患者(即瘢痕性类天疱疮患者)进行研究发现,虽然7例患者有抗基底膜自身抗体,但后者仅针对表皮基底膜中不包含表皮整联配体蛋白的区域,效价较低(即≤1:10),不与角质形成细胞外基质反应,且在人角质形成细胞提取物或培养基的免疫沉淀研究中不结合表皮整联配体蛋白(或任何其他特异性抗原)。在另外36例大疱性疾病患者或6名正常志愿者的研究中也未检测到抗表皮整联配体蛋白自身抗体。
瘢痕性类天疱疮是一种疾病表型,其中患者的自身抗体可能靶向表皮基底膜的不同成分。抗表皮整联配体蛋白自身抗体是一组患者的特异性免疫标志物,我们建议将这一疾病实体命名为抗表皮整联配体蛋白瘢痕性类天疱疮。