Bridoux Frank, Hugue Valerie, Coldefy Olivier, Goujon Jean-Michel, Bauwens Marc, Sechet Anne, Preud'Homme Jean-Louis, Touchard Guy
Department of Nephrology, and Laboratory of Immunology and Immunopathology(CNRS ESA 6031), University Hospital, Poitiers, France.
Kidney Int. 2002 Nov;62(5):1764-75. doi: 10.1046/j.1523-1755.2002.00628.x.
The clinical relevance of distinguishing two types of glomerulonephritis (GN) with non-amyloid organized immunoglobulin (Ig) deposits-fibrillary GN (FGN) and immunotactoid (microtubular) GN (IT/MTGN)-on the basis of ultrastructural organization, is debated.
Twenty-three patients with organized glomerular Ig deposits were classified into two groups based on the fibrillar or microtubular ultrastructural appearance of the deposits. Kidney biopsy samples were studied by immunofluorescence microscopy, using anti-light chain conjugates (all cases) and anti-IgG subclass conjugates (13 patients). In each group, we studied clinicopathological features, associated monoclonal gammapathy (detected by immunoelectrophoresis and/or immunoblot) or B-cell lymphoproliferative disease, effects of chemotherapy and long-term renal outcome.
In 14 IT/MTGN and 9 FGN patients, clinical symptoms [hypertension, nephrotic syndrome (NS) and hematuria] and the mean diameters of the substructures were similar. In 13 IT/MTGN patients, glomerular (IgG1, 2 or 3) deposits were monotypic (kappa, 7 cases; lambda, 6 cases). Glomerular deposits were associated with a monoclonal Ig of the same isotype in eight patients, detected in the serum (5 cases), and/or in the cytoplasm of lymphocytes (4 cases), and with lymphoproliferative disease in seven patients. The ultrastructural features of monoclonal Ig inclusions in lymphocytes were similar to those of glomerular microtubular deposits. In contrast, none of the FGN patients presented lymphoplasmocytic proliferation or paraproteinemia. Glomerular Ig deposits were polyclonal in eight cases and contained IgG4 in all three cases studied. Although patient and renal survival did not differ significantly between the two groups, chemotherapy led to remission of NS in ten IT/MTGN patients, with parallel improvement in hematological parameters.
The identification of ultrastructural patterns in these nephropathies is important. GN with organized microtubular monoclonal deposits (GOMMID) probably accounts for a large proportion of immunotactoid (microtubular) GN cases.
基于超微结构组织区分两种伴有非淀粉样有组织免疫球蛋白(Ig)沉积的肾小球肾炎(GN)——纤维样肾小球肾炎(FGN)和免疫触须样(微管样)肾小球肾炎(IT/MTGN)——的临床相关性存在争议。
23例有组织性肾小球Ig沉积的患者根据沉积物的纤维样或微管样超微结构外观分为两组。肾活检样本通过免疫荧光显微镜检查,使用抗轻链结合物(所有病例)和抗IgG亚类结合物(13例患者)。在每组中,我们研究了临床病理特征、相关单克隆丙种球蛋白病(通过免疫电泳和/或免疫印迹检测)或B细胞淋巴增殖性疾病、化疗效果和长期肾脏转归。
在14例IT/MTGN患者和9例FGN患者中,临床症状[高血压、肾病综合征(NS)和血尿]以及亚结构的平均直径相似。在13例IT/MTGN患者中,肾小球(IgG1、2或3)沉积物为单型(kappa,7例;lambda,6例)。肾小球沉积物与血清(5例)和/或淋巴细胞胞质(4例)中检测到的8例患者的相同同种型单克隆Ig相关,并且与7例患者的淋巴增殖性疾病相关。淋巴细胞中单克隆Ig包涵体的超微结构特征与肾小球微管样沉积物相似。相比之下,FGN患者均未出现淋巴细胞浆细胞增殖或副蛋白血症。8例肾小球Ig沉积物为多克隆,在所研究的3例中均含有IgG4。尽管两组患者的生存率和肾脏生存率无显著差异,但化疗使10例IT/MTGN患者的NS缓解,血液学参数同时改善。
识别这些肾病中的超微结构模式很重要。伴有有组织微管样单克隆沉积物的GN(GOMMID)可能占免疫触须样(微管样)GN病例的很大比例。