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围绕血液透析相关淀粉样沉积物的细胞主要是巨噬细胞。

Cells surrounding haemodialysis-associated amyloid deposits are mainly macrophages.

作者信息

Argilés A, Mourad G, Kerr P G, García M, Collins B, Demaille J G

机构信息

UPR 9008 CNRS/CRBM, Faculté de Medecine, Université de Montpellier I, France.

出版信息

Nephrol Dial Transplant. 1994;9(6):662-7. doi: 10.1093/ndt/9.6.662.

DOI:10.1093/ndt/9.6.662
PMID:7970093
Abstract

Dialysis-related amyloidosis is a type of amyloidosis which had beta 2-microglobulin as the major protein constituent and occurs predominantly in haemodialysis patients. Its prevalence is very high with increasing time on dialysis treatment and its pathogenesis is not completely understood. While remarkable progress has been made in the identification of the components of the deposits, there are no reports characterizing the cells surrounding the amyloid fibrils. To characterize the cellular composition of the amyloid material, specimens from seven patients treated by maintenance haemodialysis were studied with immunoperoxidase labelling using monoclonal antibodies to leukocytes (CD3, CD14, CD68, CD4, CD8, CD45). The results were very reproducible for the seven deposits assessed: Of the 182 +/- 26 leukocytes/0.2 mm2 of amyloid tissue expressing the 71.5-CD45 marker (common leukocyte), 91 +/- 6% were CD68 (KP1) positive (monocyte macrophage). No CD3-positive cells (T-cell marker) were found in six of the seven patients, with only 1.6% in the remaining one. The present study shows that although amyloidosis has classically been considered as an acellular pathology, clearly there are cells surrounding amyloid fibrils. Strikingly, these cells are almost exclusively macrophages; there are no lymphocytes or granulocytes. The putative role of macrophages in the pathogenesis of beta 2-microglobulin amyloidosis remains to be established. However, the identification and quantitation of the cells surrounding the amyloid deposits may be important for subsequent studies to elucidate amyloid pathogenesis and particularly protein-cell interactions.

摘要

透析相关性淀粉样变是一种以β2-微球蛋白为主要蛋白质成分的淀粉样变,主要发生在血液透析患者中。随着透析治疗时间的增加,其患病率非常高,其发病机制尚未完全明确。虽然在确定沉积物成分方面取得了显著进展,但尚无关于淀粉样纤维周围细胞特征的报道。为了表征淀粉样物质的细胞组成,我们使用针对白细胞的单克隆抗体(CD3、CD14、CD68、CD4、CD8、CD45),通过免疫过氧化物酶标记对7例维持性血液透析患者的标本进行了研究。对于评估的7个沉积物,结果具有很高的可重复性:在每0.2平方毫米淀粉样组织中表达71.5-CD45标记(常见白细胞)的182±26个白细胞中,91±6%为CD68(KP1)阳性(单核巨噬细胞)。7例患者中有6例未发现CD3阳性细胞(T细胞标记),其余1例仅为1.6%。本研究表明,尽管淀粉样变传统上被认为是一种无细胞病理学,但显然淀粉样纤维周围存在细胞。引人注目的是,这些细胞几乎全是巨噬细胞;没有淋巴细胞或粒细胞。巨噬细胞在β2-微球蛋白淀粉样变发病机制中的假定作用仍有待确定。然而,识别和定量淀粉样沉积物周围的细胞对于后续阐明淀粉样变发病机制尤其是蛋白质-细胞相互作用的研究可能很重要。

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Systemic amyloidosis of beta 2-microglobulin type: a complication of long-term haemodialysis.β2-微球蛋白型系统性淀粉样变性:长期血液透析的一种并发症。
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