Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
Am J Kidney Dis. 2016 Jun;67(6):949-53. doi: 10.1053/j.ajkd.2016.01.012. Epub 2016 Feb 17.
Complement-mediated glomerulonephritis, which includes C3 glomerulopathy, is characterized by dominant staining of C3 with minimal or no immunoglobulin deposits on immunofluorescence studies. We describe a new entity of complement-mediated glomerulonephritis that is characterized by bright C4d staining but with no or minimal C3 or immunoglobulin deposits on immunofluorescence studies. We label this entity as C4 glomerulopathy. C4 glomerulopathy includes C4 dense deposit disease and C4 glomerulonephritis. C4 dense deposit disease is characterized by bright C4d staining and dense deposits along glomerular basement membranes. C4 glomerulonephritis is characterized by bright C4d staining and many mesangial electron-dense deposits, with or without rare intramembranous electron-dense deposits. We describe clinical features and kidney biopsy results in a short series of 3 patients to highlight these findings. All 3 patients presented with proteinuria, and 2 patients also had hematuria. Kidney function was preserved in 2 patients, whereas 1 patient presented with declining kidney function. Evaluation for autoimmune disease, infection, and paraprotein yielded negative results in all patients. Complement levels were normal, although 1 patient had borderline low C4 levels. Kidney biopsy showed mesangial proliferative or membranoproliferative glomerulonephritis with bright C4d staining and absent or minimal C1q, C3, and immunoglobulin. Laser microdissection and mass spectrometry of glomeruli in all 3 patients showed large to moderate numbers of spectra matching C4. Furthermore, analysis of amino acid sequences showed that they were localized to the C4d portion of C4, consistent with immunofluorescence findings. Further studies are required to determine the underlying cause. In summary, we describe a novel complement-mediated glomerulonephritis that is characterized by bright glomerular C4d staining with minimal or absent staining for C1q, C3, and immunoglobulin.
补体介导的肾小球肾炎,包括 C3 肾小球病,其特征是免疫荧光研究中 C3 染色明显,而免疫球蛋白沉积很少或没有。我们描述了一种新的补体介导的肾小球肾炎实体,其特征是 C4d 染色明亮,但免疫荧光研究中 C3 或免疫球蛋白沉积很少或没有。我们将这种实体标记为 C4 肾小球病。C4 肾小球病包括 C4 致密物沉积病和 C4 肾小球肾炎。C4 致密物沉积病的特征是 C4d 染色明亮,沿肾小球基底膜有致密沉积物。C4 肾小球肾炎的特征是 C4d 染色明亮,有许多系膜电子致密沉积物,有或没有罕见的内皮下电子致密沉积物。我们描述了 3 例短系列患者的临床特征和肾活检结果,以突出这些发现。所有 3 例患者均表现为蛋白尿,其中 2 例患者也有血尿。2 例患者的肾功能正常,而 1 例患者的肾功能下降。所有患者的自身免疫性疾病、感染和副蛋白评估均为阴性。补体水平正常,尽管 1 例患者 C4 水平临界降低。肾活检显示系膜增生性或膜增生性肾小球肾炎,C4d 染色明亮,C1q、C3 和免疫球蛋白缺失或很少。3 例患者的肾小球激光微切割和质谱分析显示大量至中等数量的谱与 C4 匹配。此外,氨基酸序列分析表明它们定位于 C4 的 C4d 部分,与免疫荧光结果一致。需要进一步研究以确定潜在的原因。总之,我们描述了一种新的补体介导的肾小球肾炎,其特征是肾小球 C4d 染色明亮,而 C1q、C3 和免疫球蛋白染色很少或没有。