Yusa A, Saito T, Soma J, Ootaka T, Sato H, Abe K
Second Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
Nihon Jinzo Gakkai Shi. 1996 Jun;38(6):239-47.
We investigated infiltrating cells in the glomeruli and interstitium in biopsy specimens from 41 cases with membranous nephropathy (MN) and found that 21 had focal segmental glomerulosclerosis (FGS) and 20 did not. There was no significant difference between groups MN +FGS and MN regarding age, interval from onset, serum creatinine level and urine protein excretion when the biopsy was performed. The cells were analyzed with 3-layer indirect immunoperoxidase techniques using monoclonal antibodies to leukocyte common antigen, T cells, B cells and monocytes/macrophages (Mo/M phi). The numbers of leukocytes in both glomeruli and interstitium increased significantly in group MN+FGS as compared to those in group MN, respectively. Most of the leukocytes infiltrating the glomeruli were Mo/M phi, while T cells and Mo/M phi were predominant in the interstitium. There was a significant correlation between the numbers of intraglomerular and interstitial Mo/M phi in group MN+FGS, but not in group MN. Follow-up periods after the biopsy were not significantly different between the groups. At the final points of follow-up, urine protein excretion significantly decreased in group MN, but not in group MN+FGS. In group MN+FGS, serum creatinine levels were twice the level found at the biopsy in 5 cases, and 2 required hemodialysis therapy. Renal functions were not deteriorated in any cases of group MN. These findings suggest that FGS may be one the deleterious factors in MN, which may facilitate the infiltration of Mo/M phi in both glomeruli and interstitium and T cells in the interstitium.
我们研究了41例膜性肾病(MN)活检标本中肾小球和间质的浸润细胞,发现其中21例有局灶节段性肾小球硬化(FGS),20例没有。MN+FGS组和MN组在年龄、起病间隔、血清肌酐水平及活检时的尿蛋白排泄方面无显著差异。采用针对白细胞共同抗原、T细胞、B细胞及单核细胞/巨噬细胞(Mo/M phi)的单克隆抗体,通过三层间接免疫过氧化物酶技术对细胞进行分析。与MN组相比,MN+FGS组肾小球和间质中的白细胞数量均显著增加。浸润肾小球的白细胞大多为Mo/M phi,而间质中T细胞和Mo/M phi占主导。MN+FGS组肾小球内和间质中Mo/M phi的数量之间存在显著相关性,而MN组则无。两组活检后的随访期无显著差异。在随访终点,MN组尿蛋白排泄显著下降,而MN+FGS组则未下降。在MN+FGS组,5例患者的血清肌酐水平是活检时的两倍,2例需要血液透析治疗。MN组所有病例的肾功能均未恶化。这些发现提示,FGS可能是MN中的有害因素之一,它可能促进Mo/M phi在肾小球和间质以及T细胞在间质中的浸润。