Ward H J, Koyle M A
Division of Nephrology, Harbor-U.C.L.A. Medical Center, Torrance, CA 90509.
Transplantation. 1988 Mar;45(3):524-9. doi: 10.1097/00007890-198803000-00004.
De novo membranous nephropathy (MN) is now one of the most common forms of posttransplant glomerular disease, second only to allograft glomerulopathy. We investigated several immunopathologic and physicochemical properties of the immune complex (IC) or IC components displayed in the sera of patients with de novo MN. The parameters studied included detection of small (9S) preformed IC by monoclonal rheumatoid factor, determination of IC isoelectric point by chromatofocusing, detection of cationic IgG spectrotypes (pI 8.0-9.2), and demonstration of brush border or tubular epithelial/interstitial antibodies in the sera by indirect immunofluorescence. Of 7 de novo MN sera, 5 demonstrated the presence of each of these four immunopathologic features, whereas normal transplant patients, transplant recipients with recurrent focal sclerosis (FSGN), and those with chronic rejection did not display such features. Sera of patients with untreated idiopathic MN revealed immunochemical properties of IC that were similar to those seen in circulating IC of de novo MN. These studies suggest that a strongly nephritogenic internal milieu exists in transplant recipients with de novo MN. Our data indicate that unique immunochemical properties of IC or their components may predispose to subepithelial immune deposit formation and should provide new insights into the pathogenesis of idiopathic human MN.
新发膜性肾病(MN)现已成为移植后肾小球疾病最常见的形式之一,仅次于同种异体移植肾小球病。我们研究了新发MN患者血清中显示的免疫复合物(IC)或IC成分的几种免疫病理和物理化学特性。所研究的参数包括用单克隆类风湿因子检测小(9S)预形成IC、通过层析聚焦法测定IC的等电点、检测阳离子IgG光谱类型(pI 8.0 - 9.2)以及通过间接免疫荧光法在血清中显示刷状缘或肾小管上皮/间质抗体。在7份新发MN血清中,5份显示出这四种免疫病理特征中的每一种,而正常移植患者、复发性局灶节段性肾小球硬化(FSGN)移植受者以及慢性排斥患者均未表现出此类特征。未经治疗的特发性MN患者的血清显示出IC的免疫化学特性,与新发MN循环IC中所见的特性相似。这些研究表明,新发MN的移植受者中存在强烈的致肾炎内部环境。我们的数据表明,IC或其成分独特的免疫化学特性可能易导致上皮下免疫沉积物形成,并应为特发性人类MN的发病机制提供新的见解。