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活动性溃疡性结肠炎患者血清血栓调节蛋白水平升高及免疫组化表达降低。

Elevated serum levels and reduced immunohistochemical expression of thrombomodulin in active ulcerative colitis.

作者信息

Boehme M W, Autschbach F, Zuna I, Scherbaum W A, Stange E, Raeth U, Sieg A, Stremmel W

机构信息

Department of Internal Medicine IV, University of Heidelberg, Germany.

出版信息

Gastroenterology. 1997 Jul;113(1):107-17. doi: 10.1016/s0016-5085(97)70086-6.

Abstract

BACKGROUND & AIMS: The pathogenesis of ulcerative colitis and Crohn's disease is still unclear. Vascular injury has been suggested as a potential pathogenetic mechanism. Serum thrombomodulin is a marker of endothelial cell injury. The aim of this study was to determine the relevance of increased serum thrombomodulin levels for assessing disease activity in inflammatory bowel disease. As a potential cause of serum thrombomodulin level increase, the loss of local vascular thrombomodulin expression was investigated immunohistochemically.

METHODS

Thrombomodulin levels were determined by enzyme-linked immunosorbent assay in sera from patients with ulcerative colitis, Crohn's disease, Schistosoma mansoni infection, and infectious diarrhea and controls. The vascular expression of thrombomodulin was investigated immunohistochemically in fresh frozen transmural specimens of normal, Crohn's, and ulcerative colitis bowel samples.

RESULTS

Significantly elevated serum thrombomodulin levels were only detected in active ulcerative colitis and infectious diarrhea complicated by septicemia. A marked and general loss of vascular endothelial cell thrombomodulin expression was found immunohistochemically in inflamed bowel tissues. Graded by a newly established thrombomodulin staining index, this was significantly more marked in ulcerative colitis than Crohn's disease.

CONCLUSIONS

Serum thrombomodulin proved to be a novel marker of disease activity in ulcerative colitis closely related to local vascular endothelial cell damage, which might be a relevant pathophysiological feature of ulcerative colitis.

摘要

背景与目的

溃疡性结肠炎和克罗恩病的发病机制仍不明确。血管损伤被认为是一种潜在的发病机制。血清血栓调节蛋白是内皮细胞损伤的标志物。本研究的目的是确定血清血栓调节蛋白水平升高与评估炎症性肠病疾病活动度的相关性。作为血清血栓调节蛋白水平升高的潜在原因,通过免疫组织化学方法研究局部血管血栓调节蛋白表达的缺失情况。

方法

采用酶联免疫吸附测定法测定溃疡性结肠炎、克罗恩病、曼氏血吸虫感染、感染性腹泻患者及对照者血清中的血栓调节蛋白水平。采用免疫组织化学方法研究正常、克罗恩病和溃疡性结肠炎肠组织新鲜冰冻透壁标本中血栓调节蛋白的血管表达情况。

结果

仅在活动期溃疡性结肠炎和并发败血症的感染性腹泻患者中检测到血清血栓调节蛋白水平显著升高。免疫组织化学研究发现,在炎症肠组织中血管内皮细胞血栓调节蛋白表达明显且普遍缺失。根据新建立的血栓调节蛋白染色指数分级,溃疡性结肠炎中的这种情况比克罗恩病更明显。

结论

血清血栓调节蛋白被证明是溃疡性结肠炎疾病活动度的一种新标志物,与局部血管内皮细胞损伤密切相关,这可能是溃疡性结肠炎的一个相关病理生理特征。

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