Medizinische Poliklinik Campus Innenstadt, University of Munich, 80336 Munich, Germany.
Hum Pathol. 2010 Apr;41(4):582-93. doi: 10.1016/j.humpath.2009.08.024. Epub 2009 Dec 11.
The Alport syndrome is a hereditary glomerular disease linked to structural abnormalities of collagen IV. In a mouse model of Alport syndrome, the interstitial lymphocyte influx was important for disease progression. CXCR3 is a chemokine receptor involved in lymphocyte recruitment to the kidney. We hypothesized that CXCR3-positive T cells might be involved in human Alport syndrome. Immunohistochemistry was performed on formalin-fixed, paraffin-embedded biopsies from 17 patients with Alport syndrome, 10 with immunoglobulin A (IgA) nephropathy, and 11 healthy donor kidneys. We investigated the expression of the alpha5 chain of collagen IV to confirm the morphologic diagnosis, the chemokine receptor CXCR3 and CD3-positive T cells. Alport syndrome biopsies demonstrated a complete loss of the alpha5 chain of collagen IV from the glomerular basement membrane and the morphologic features consistent with Alport syndrome on electron microscopy. A prominent number of CXCR3-positive cells were found in the tubulointerstitium. Most of the CXCR3-positive cells were CD3-positive T cells, demonstrated by double-labeling in selected biopsies. The number of CXCR3-positive cells in kidneys with Alport syndrome correlated with serum creatinine (P < .05) and with morphologic features of a progressive disease (eg, interstitial fibrosis, glomerulosclerosis, and tubular atrophy). The severity of interstitial CXCR3-positive cell influx was similar in Alport syndrome as compared to immunoglobulin A nephropathy. The noninflammatory glomerular lesion of Alport syndrome is associated with prominent interstitial accumulation of CD3- and CXCR3-positive lymphocytes. The degree of infiltration correlated with renal function. We speculate that targeting T lymphocytes, for example, by CXCR3 blocking agents, might be a novel approach to inhibit disease progression in patients with Alport syndrome.
遗传性肾小球疾病 Alport 综合征与 IV 型胶原的结构异常有关。在 Alport 综合征的小鼠模型中,间质淋巴细胞浸润对疾病进展很重要。CXCR3 是一种趋化因子受体,参与淋巴细胞向肾脏的募集。我们假设 CXCR3 阳性 T 细胞可能参与人类 Alport 综合征。对 17 例 Alport 综合征、10 例免疫球蛋白 A(IgA)肾病和 11 例健康供体肾脏的福尔马林固定、石蜡包埋活检进行了免疫组织化学染色。我们检测了 IV 型胶原 α5 链的表达以确认形态学诊断,检测了趋化因子受体 CXCR3 和 CD3 阳性 T 细胞。Alport 综合征活检显示肾小球基底膜完全缺失 IV 型胶原 α5 链,电镜下具有 Alport 综合征的形态学特征。在肾小管间质中发现大量 CXCR3 阳性细胞。在选定的活检中通过双重标记显示,大多数 CXCR3 阳性细胞为 CD3 阳性 T 细胞。Alport 综合征肾脏中 CXCR3 阳性细胞的数量与血清肌酐(P<0.05)和进行性疾病的形态学特征(如间质纤维化、肾小球硬化和肾小管萎缩)相关。Alport 综合征与 IgA 肾病相比,间质 CXCR3 阳性细胞浸润的严重程度相似。Alport 综合征的非炎症性肾小球病变与 CD3 和 CXCR3 阳性淋巴细胞的明显间质积聚有关。浸润程度与肾功能相关。我们推测,例如通过 CXCR3 阻断剂靶向 T 淋巴细胞可能是抑制 Alport 综合征患者疾病进展的新方法。