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分泌性免疫系统与肾脏疾病。

The secretory immune system and renal disease.

作者信息

Dobrin R S, Knudson F E, Michael A F

出版信息

Clin Exp Immunol. 1975 Aug;21(2):318-28.

Abstract

An immunopathological analysis of renal tissue from 105 patients was undertaken: (1) to clarify the relationship of the secretory immune system to renal diseases in which glomerular deposits of immunoglobulin A, (alpha chain), occurred; (2) to determine the lower nephron localization of secretory component and alpha chain in renal disease. This study, which included twenty-four patients with glomerular deposits of alpha chain, failed to reveal glomerular localization of secretory IgA. Secretory component was not found in renal tubular cells in kidneys with normal or minimally abnormal renal histology. In contradistinction to these findings, significant amounts of secretory component were found in tubular epithelial cells and casts in tissue from fifty-one patients with morphological evidence of significant renal damage; this localization had no correlation with glomerular deposits of IgA, IgM or other immunoreactants. Alpha Chain was rarely found in the tubular epithelium or in interstitial round cells; fifteen patients had alpha chain in casts. We conclude that the glomerular localization of immunoglobulin in glomerulonephritis is not derived from the secretory immune system, and the IgA present in glomeruli is not secretory IgA. The finding of secretory component in tubular cells in diseased kidneys without alpha chain may support an hypothesis for an independent role for secretory component in renal disease, apart from its function in the transport and stabilization of secretory IgA.

摘要

对105例患者的肾组织进行了免疫病理学分析:(1)阐明分泌免疫系统与免疫球蛋白A(α链)在肾小球沉积的肾脏疾病之间的关系;(2)确定分泌成分和α链在肾脏疾病中的肾单位远端定位。本研究包括24例α链在肾小球沉积的患者,未发现分泌型IgA的肾小球定位。在肾脏组织学正常或轻度异常的肾脏中,肾小管细胞未发现分泌成分。与这些发现相反,在51例有明显肾脏损害形态学证据的患者组织中,肾小管上皮细胞和管型中发现了大量分泌成分;这种定位与IgA、IgM或其他免疫反应物的肾小球沉积无关。α链很少在肾小管上皮或间质圆形细胞中发现;15例患者的管型中有α链。我们得出结论,肾小球肾炎中免疫球蛋白的肾小球定位并非来自分泌免疫系统,肾小球中存在的IgA不是分泌型IgA。在无α链的患病肾脏的肾小管细胞中发现分泌成分,这可能支持一种假说,即分泌成分在肾脏疾病中具有独立作用,与其在分泌型IgA的转运和稳定中的功能无关。

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