Jennette J C, Lamanna R W, Burnette J P, Wilkman A S, Iskander S S
Am J Clin Pathol. 1982 Sep;78(3):381-6. doi: 10.1093/ajcp/78.3.381.
A teenage male, with Goodpasture's syndrome and serum antiglomerular basement membrane (anti-GBM) antibodies, had a focal proliferative glomerulonephritis with crescents. Immunofluorescence microscopy of his glomeruli using anti-IgG antibodies demonstrated both intense linear GBM staining, and granular subepithelial staining. Electron microscopy revealed numerous subepithelial electron-dense deposits. Identical IgG subclass restriction (dominance of IgG1 and IgG4) of both types of glomerular deposits in this patient supports, but does not prove, a postulate that the linear staining was due to anti-GBM antibodies bound to intact GBM, and that the granular staining was due to anti-GBM antibodies complexed with freed GBM antigens.
一名患有古德帕斯彻综合征并伴有血清抗肾小球基底膜(anti-GBM)抗体的青少年男性,患有局灶性增生性肾小球肾炎伴新月体形成。使用抗IgG抗体对其肾小球进行免疫荧光显微镜检查显示,肾小球基底膜(GBM)呈强烈线性染色,以及上皮下颗粒状染色。电子显微镜检查发现大量上皮下电子致密沉积物。该患者两种类型的肾小球沉积物具有相同的IgG亚类限制(IgG1和IgG4占优势),这支持但未证明一种假设,即线性染色是由于抗GBM抗体与完整的GBM结合,而颗粒状染色是由于抗GBM抗体与游离的GBM抗原形成复合物。