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人肾移植中诱导性淋巴细胞共刺激分子的表达

Expression of inducible lymphocyte costimulatory molecules in human renal allograft.

作者信息

Biancone L, Segoloni G, Turello E, Donati D, Bussolati B, Piccoli G, Camussi G

机构信息

Dipartimento di Scienze Cliniche e Biologiche, Università di Pavia, Varese, Italy.

出版信息

Nephrol Dial Transplant. 1998 Mar;13(3):716-22. doi: 10.1093/ndt/13.3.716.

DOI:10.1093/ndt/13.3.716
PMID:9550652
Abstract

BACKGROUND

CTLA-4/CD28-B7 and CD40-CD40L interactions constitute two key costimulatory pathways in lymphocyte signalling during experimental allograft rejection. Studies on the expression of these molecules in human transplant rejection are still lacking.

METHODS

The immunohistochemical study was performed on renal biopsies obtained for various clinical complications from 25 renal transplant patients. Expression of B7-1 and B7-2 and their counter-receptor CTLA-4, and of CD40 and its counter-receptor CD40L was examined.

RESULTS

In acute rejection a focal intense infiltration of B7-1+ and B7-2+ cells (mainly CD20- CD14+) and of CTLA-4+ T lymphocytes (mainly CD8+) was present. In contrast, CD40 and CD40L were rarely expressed. Accumulations of T lymphocytes were found in the interstitium in the same area containing B7-1+ and B7-2+ cells. The scattered CD40L+ cells found in the T-cell infiltrate exhibited the CD4+ phenotype. In chronic rejection only a few B7-1+, B7-2+ or CTLA-4+ cells were detectable. In contrast, several CD40L+CD4+ cells were present both in the interstitium and in glomeruli. Moreover, an intense expression of CD40 on the endothelium was observed. In patients with cyclosporin nephrotoxicity cells positive for B7-1, B7 2, CTLA-4, CD40, or CD40L were absent.

CONCLUSIONS

These results demonstrate a differential expression of costimulatory molecules in renal biopsies of allograft recipients undergoing acute or chronic rejection. Moreover, their detection may prove useful to discriminate rejection from cyclosporin nephrotoxicity.

摘要

背景

CTLA-4/CD28-B7和CD40-CD40L相互作用构成了实验性同种异体移植排斥反应中淋巴细胞信号传导的两个关键共刺激途径。关于这些分子在人类移植排斥反应中的表达研究仍很缺乏。

方法

对25例肾移植患者因各种临床并发症获取的肾活检组织进行免疫组织化学研究。检测B7-1和B7-2及其共受体CTLA-4,以及CD40及其共受体CD40L的表达。

结果

在急性排斥反应中,存在B7-1+和B7-2+细胞(主要为CD20-CD14+)以及CTLA-4+T淋巴细胞(主要为CD8+)的局灶性强烈浸润。相比之下,CD40和CD40L很少表达。在含有B7-1+和B7-2+细胞的同一区域的间质中发现了T淋巴细胞聚集。在T细胞浸润中发现的散在的CD40L+细胞表现出CD4+表型。在慢性排斥反应中,仅可检测到少数B7-1+、B7-2+或CTLA-4+细胞。相比之下,间质和肾小球中均存在一些CD40L+CD4+细胞。此外,观察到内皮细胞上CD40的强烈表达。在环孢素肾毒性患者中,未发现B7-1、B7-2、CTLA-4、CD40或CD40L阳性细胞。

结论

这些结果表明,在经历急性或慢性排斥反应的同种异体移植受者的肾活检组织中,共刺激分子存在差异表达。此外,它们的检测可能有助于区分排斥反应和环孢素肾毒性。

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