Tatnall F M, Whitehead P C, Black M M, Wojnarowska F, Leigh I M
Department of Experimental Dermatology, London Hospital, U.K.
Br J Dermatol. 1989 Apr;120(4):533-9. doi: 10.1111/j.1365-2133.1989.tb01327.x.
The sera from two patients with epidermolysis bullosa acquisita were blotted against dermal extracts in comparison with the mouse monoclonal antibody LH 7.2. This antibody reacts with carboxy terminal region of type VII collagen. The epidermolysis bullosa acquisita antisera showed binding to the same molecular weight protein as LH 7.2 confirming that the target antigen for epidermolysis bullosa acquisita antibodies is the carboxy terminal region of type VII collagen. This newly described collagen forms the major component of anchoring fibrils. These findings are consistent with established ultrastructural data which have shown that the epidermolysis bullosa acquisita antigen is located within and below the lamina densa. The monoclonal antibody LH 7.2 provides an internal standard for epidermolysis bullosa acquisita autoantisera activity. The use of immunoblotting of epidermolysis bullosa autoantisera in comparison with the monoclonal antibody LH 7.2 provides definitive investigation for the diagnosis of this disorder.
将两名获得性大疱性表皮松解症患者的血清与小鼠单克隆抗体LH 7.2一起,针对真皮提取物进行印迹分析。该抗体与VII型胶原的羧基末端区域发生反应。获得性大疱性表皮松解症抗血清显示与LH 7.2结合相同分子量的蛋白质,证实获得性大疱性表皮松解症抗体的靶抗原是VII型胶原的羧基末端区域。这种新描述的胶原形成了锚定原纤维的主要成分。这些发现与已有的超微结构数据一致,这些数据表明获得性大疱性表皮松解症抗原位于致密板层内和下方。单克隆抗体LH 7.2为获得性大疱性表皮松解症自身抗血清活性提供了一个内部标准。将获得性大疱性表皮松解症自身抗血清与单克隆抗体LH 7.2进行免疫印迹分析,为该疾病的诊断提供了确定性的研究方法。