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与抗肾基底膜抗体相关的人类肾小管间质性肾炎的组织学

Histology of human tubulo-interstitial nephritis associated with antibodies to renal basement membranes.

作者信息

Andres G, Brentjens J, Kohli R, Anthone R, Anthone S, Baliah T, Montes M, Mookerjee B K, Prezyna A, Sepulveda M, Venuto R, Elwood C

出版信息

Kidney Int. 1978 Jun;13(6):480-91. doi: 10.1038/ki.1978.71.

Abstract

Twenty-seven patients with diffuse "crescentic" glomerulonephritis (CSGN) were identified in 1,174 renal biopsies from nephritic patients. Patients were assigned to three groups on the basis of the immunofluorescent study of renal biopsy specimens and serologic findings. Group I included eight patients with antibodies to glomerular (anti-GBM) and tubular (anti-TBM) basement membranes; group II had eight patients with only anti-GBM antibodies; and group III had eleven patients with CSGN unassociated with antibodies to either GBM or TBM. Patients with anti-GBM/anti-TBM antibodies (group I) had severe tubulointerstitial (TI) nephritis, as characterized by the infiltration of polymorphonuclear leukocytes and macrophages along the TBM and peritubular vessels. In some patients, focal proliferation of epithelial cells of proximal convoluted tubules (PCT), gaps or extensive destruction of TBM, lesions in the walls of small peritubular vessels, and interstitial giant cells were also observed. Patients with anti-GBM antibodies (group II) had mild to moderate interstitial cellular infiltration and mild tubular changes. Five patients with CSGN not associated with antibodies to renal basement membranes (group III) had mild to moderate interstitial cellular infiltration and tubular changes. A sixth patient, with Wegener's disease had severe granulomatous TI lesions. The results of this study show that TI nephritis is most frequent and severe with anti-TBM antibodies are demonstrable and suggest that anti-TBM antibodies contribute to the development of TI lesions.

摘要

在1174例肾炎患者的肾活检中,确诊了27例弥漫性“新月体性”肾小球肾炎(CSGN)患者。根据肾活检标本的免疫荧光研究和血清学检查结果,将患者分为三组。第一组包括8例有肾小球(抗GBM)和肾小管(抗TBM)基底膜抗体的患者;第二组有8例仅有抗GBM抗体的患者;第三组有11例CSGN患者,其与GBM或TBM抗体均无关。有抗GBM/抗TBM抗体的患者(第一组)患有严重的肾小管间质(TI)肾炎,其特征为沿TBM和肾小管周围血管有多形核白细胞和巨噬细胞浸润。在一些患者中,还观察到近端小管(PCT)上皮细胞局灶性增生、TBM间隙或广泛破坏、肾小管周围小血管壁病变以及间质巨细胞。有抗GBM抗体的患者(第二组)有轻度至中度间质细胞浸润和轻度肾小管改变。5例与肾基底膜抗体无关的CSGN患者(第三组)有轻度至中度间质细胞浸润和肾小管改变。第六例患有韦格纳肉芽肿病的患者有严重的肉芽肿性TI病变。本研究结果表明,TI肾炎在可检测到抗TBM抗体时最为常见且严重,并提示抗TBM抗体促成了TI病变的发展。

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