Vizjak Alenka, Rott Tomaz, Koselj-Kajtna Mira, Rozman Blaz, Kaplan-Pavlovcic Stasa, Ferluga Dusan
Institute of Pathology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Am J Kidney Dis. 2003 Mar;41(3):539-49. doi: 10.1053/ajkd.2003.50142.
The major antigen specificities of antineutrophil cytoplasmic antibodies (ANCA) are for proteinase 3 (PR3) and myeloperoxidase (MPO). Only a limited number of studies have systematically assessed renal pathology with respect to ANCA antigen specificity.
The authors evaluated renal biopsy light microscopy and immunofluorescence findings, clinical presentation, and outcome in 135 patients with ANCA-associated vasculitides.
Patients were divided into 3 groups: PR3-ANCA (n = 55), MPO-ANCA (n = 74), and ANCA of other specificities (n = 6). The mean duration of renal disease at biopsy was significantly longer in patients with MPO-ANCA than in those with PR3-ANCA (6.9 v 3.0 months). Immunofluorescence results showed mostly pauci-immune glomerulonephritis (n = 129) and rarely diffuse granular glomerular immune deposits suggesting immune complex deposition (n = 6). A focal form of crescentic glomerulonephritis was more frequent (P < 0.001), and glomerular necrosis was more prominent (P = 0.013) in the PR3-ANCA group, whereas diffuse crescentic glomerulonephritis, glomerulosclerosis, and interstitial fibrosis predominated in the MPO-ANCA group (P < 0.001). Extraglomerular vasculitis, present in 22.2%, and chronic vascular lesions indicative of previous vasculitis, present in 11.9% of patients, correlated with systemic involvement.
The evolution of the pathologic lesions of PR3-ANCA and MPO-ANCA-associated glomerulonephritis seems to be similar. Differences in histopathology could be explained by the observation that in patients with PR3-ANCA, kidney biopsy was performed soon after renal involvement appeared, and focal active lesions were prevalent, whereas in patients with MPO-ANCA, kidney biopsy was done late in the course of the disease, and diffuse chronic sclerotic lesions predominated. Renal extraglomerular small vessel vasculitis appeared to be predictive of systemic involvement.
抗中性粒细胞胞浆抗体(ANCA)的主要抗原特异性针对蛋白酶3(PR3)和髓过氧化物酶(MPO)。仅有有限数量的研究系统地评估了与ANCA抗原特异性相关的肾脏病理学。
作者评估了135例ANCA相关性血管炎患者的肾活检光镜和免疫荧光结果、临床表现及预后。
患者被分为3组:PR3-ANCA组(n = 55)、MPO-ANCA组(n = 74)和其他特异性ANCA组(n = 6)。MPO-ANCA患者肾活检时肾病的平均病程显著长于PR3-ANCA患者(6.9个月对3.0个月)。免疫荧光结果显示大多为寡免疫性肾小球肾炎(n = 129),很少有提示免疫复合物沉积的弥漫性颗粒状肾小球免疫沉积物(n = 6)。局灶性新月体性肾小球肾炎在PR3-ANCA组更常见(P < 0.001),肾小球坏死更突出(P = 0.013),而弥漫性新月体性肾小球肾炎、肾小球硬化和间质纤维化在MPO-ANCA组占主导(P < 0.001)。22.2%的患者存在肾外血管炎,11.9%的患者存在提示既往血管炎的慢性血管病变,二者均与全身受累相关。
PR3-ANCA和MPO-ANCA相关性肾小球肾炎的病理病变演变似乎相似。组织病理学差异可解释为,PR3-ANCA患者在肾脏受累后不久即进行肾活检,局灶性活动性病变普遍,而MPO-ANCA患者在疾病病程后期进行肾活检,弥漫性慢性硬化性病变占主导。肾外小血管血管炎似乎可预测全身受累情况。