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肠道致病性大肠杆菌、溶菌酶和α-1-抗糜蛋白酶对泌尿生殖系统软斑病巨噬细胞的抗原性

Antigenicities of enteropathogenic Escherichia coli, lysozyme, and alpha-1-antichymotrypsin on macrophages of genitourinary malacoplakia.

作者信息

Joh K, Aizawa S, Furusato M, Shishikura Y, Itoh K, Komiya M, Hayashi H

机构信息

Department of Pathology, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Pathol Int. 1995 Mar;45(3):215-26. doi: 10.1111/j.1440-1827.1995.tb03445.x.

Abstract

Seven cases of genito-urinary malacoplakia were analyzed histologically, ultrastructurally and immunohistochemically in a comparison with two cases of xanthogranulomatous pyelonephritis. Immunohistochemically, von Hansemann cells and Michaelis-Guttmann bodies, both hallmarks for the diagnosis of malacoplakia, showed a common antigenicity for enteropathogenic Escherichia coli as cytoplasmic granules of varying sizes. These microscopic manifestations corresponded ultrastructurally to a series of phagolysosomal degradations of coliform bacilli. Serogroups against E. coli OK antigens, which were positive for malacoplakic cells, were not confined to a particular group. Macrophages of xanthogranulomatous pyelonephritis did not show the E. coli antigenicity. Antigenicity of lysozyme and alpha-1-antichymotrypsin on the von Hansemann cells was equivocal, but these enzymes were strongly positive on macrophages of xanthogranulomatous pyelonephritis. The macrophages of both malacoplakia and xanthogranulomatous pyelonephritis were positive for antihuman macrophage antibody. These results indicate that malacoplakia depends mainly on infection by a non-specific strain of enteropathogenic E. coli and may arise from defective digestive enzyme activity of infiltrating macrophages. Immunohistochemical analysis using antisera against E. coli OK antigens, lysozyme and alpha-1-antichymotrypsin was useful in identifying the prediagnostic stage of malacoplakia and in differentiating the lesion from xanthogranulomatous pyelonephritis.

摘要

对7例泌尿生殖系统软斑病进行了组织学、超微结构和免疫组织化学分析,并与2例黄色肉芽肿性肾盂肾炎进行比较。免疫组织化学显示,作为软斑病诊断标志的von Hansemann细胞和Michaelis-Guttmann小体,对致病性大肠杆菌具有共同抗原性,表现为大小不一的胞质颗粒。这些微观表现超微结构上对应于一系列大肠埃希菌的吞噬溶酶体降解。软斑病细胞呈阳性的针对大肠杆菌OK抗原的血清群并不局限于某一特定菌群。黄色肉芽肿性肾盂肾炎的巨噬细胞未显示大肠杆菌抗原性。von Hansemann细胞上溶菌酶和α-1抗糜蛋白酶的抗原性不明确,但这些酶在黄色肉芽肿性肾盂肾炎的巨噬细胞上呈强阳性。软斑病和黄色肉芽肿性肾盂肾炎的巨噬细胞抗人巨噬细胞抗体均呈阳性。这些结果表明,软斑病主要取决于致病性大肠杆菌非特异性菌株的感染,可能源于浸润巨噬细胞消化酶活性缺陷。使用抗大肠杆菌OK抗原、溶菌酶和α-1抗糜蛋白酶的抗血清进行免疫组织化学分析,有助于识别软斑病的诊断前阶段,并将该病变与黄色肉芽肿性肾盂肾炎区分开来。

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