Antigenic targets in epimembranous glomerulonephritis. Experimental data and potential application in human pathology.

Applied pathology Pub Date : 1989-01-01
P Ronco, L Allegri, E Brianti, F Chatelet, E H Van Leer, P Verroust
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Abstract

Although membranous glomerulonephritis (MGN) has been long considered as a prototype of glomerulonephritis (GN) due to the deposition of circulating immune complexes (CIC), a growing body of evidence indicates that immune deposits can also be formed in situ and implicate antigens expressed by glomerular epithelial cells (GEC). Some of these antigens have recently been identified. The first one, gp330 - a 330-kd glycoprotein restricted to the coated pits of GEC and renal brush border (BB) - is responsible for Heymann nephritis, a rat model of MGN. However, it is absent in the human glomerulus and is therefore probably not involved in human cases of MGN, at least in those due to in situ formation of CIC. In addition, by raising monoclonal antibodies against rat and rabbit BB, we have isolated two other BB proteins also expressed on GEC. The latter, respectively identified as dipeptidyl peptidase IV (90 kd) and enkephalinase (85 kd), can serve as targets for the formation of short-lived immune deposits. Since they are also detected on human GEC, they might play a role in the pathogenesis of MGN in man.

膜外肾小球肾炎的抗原靶点。实验数据及其在人体病理学中的潜在应用。
尽管膜性肾小球肾炎(MGN)一直被认为是肾小球肾炎(GN)的原型,由于循环免疫复合物(CIC)的沉积,越来越多的证据表明免疫沉积也可以在原位形成,并涉及肾小球上皮细胞(GEC)表达的抗原。最近发现了其中一些抗原。第一种是gp330,这是一种330-kd的糖蛋白,局限于GEC和肾刷状边界(BB)的包被窝,它与海曼肾炎(MGN大鼠模型)有关。然而,它在人类肾小球中不存在,因此可能与人类MGN病例无关,至少在那些由于原位CIC形成的病例中是如此。此外,通过培养抗大鼠和兔BB的单克隆抗体,我们分离到了另外两个同样在GEC上表达的BB蛋白。后者分别被鉴定为二肽基肽酶IV (90 kd)和脑啡肽酶(85 kd),可以作为短期免疫沉积形成的靶点。由于它们也在人类GEC中检测到,它们可能在人类MGN的发病机制中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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