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Fecal lactoferrin as a marker for disease activity in inflammatory bowel disease: comparison with other neutrophil-derived proteins.粪便乳铁蛋白作为炎症性肠病疾病活动的标志物:与其他中性粒细胞衍生蛋白的比较。
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Detection of decay-accelerating factor in stool specimens of patients with colorectal cancer.
Gastroenterology. 1995 Sep;109(3):826-31. doi: 10.1016/0016-5085(95)90390-9.
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Enhanced expression of decay accelerating factor and CD59/homologous restriction factor 20 on the colonic epithelium of ulcerative colitis.溃疡性结肠炎结肠上皮细胞上衰变加速因子和CD59/同源限制因子20的表达增强。
Lab Invest. 1995 May;72(5):587-91.
7
Distribution of complement regulatory proteins, decay-accelerating factor, CD59/homologous restriction factor 20 and membrane cofactor protein in human colorectal adenoma and cancer.补体调节蛋白、衰变加速因子、CD59/同源限制因子20和膜辅助因子蛋白在人大肠腺瘤和癌中的分布
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Release of GPI-anchored membrane proteins by a cell-associated GPI-specific phospholipase D.细胞相关的糖基磷脂酰肌醇特异性磷脂酶 D 释放糖基磷脂酰肌醇锚定膜蛋白。
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Decay-accelerating factor on human umbilical vein endothelial cells. Its histamine-induced expression and spontaneous rapid shedding from the cell surface.人脐静脉内皮细胞上的衰变加速因子。其组胺诱导的表达及从细胞表面的自发快速脱落
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粪便标本中的衰变加速因子(DAF)作为溃疡性结肠炎(UC)患者疾病活动的标志物。

Decay-accelerating factor (DAF) in stool specimens as a marker of disease activity in patients with ulcerative colitis (UC).

作者信息

Inaba T, Mizuno M, Ohya S, Kawada M, Uesu T, Nasu J, Takeuchi K, Nakagawa M, Okada H, Fujita T, Tsuji T

机构信息

First Department of Internal Medicine, Okayama University Medical School, Japan.

出版信息

Clin Exp Immunol. 1998 May;112(2):237-41. doi: 10.1046/j.1365-2249.1998.00573.x.

DOI:10.1046/j.1365-2249.1998.00573.x
PMID:9649185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1904958/
Abstract

Colonic epithelial cells of patients with UC express DAF in relation to the severity of mucosal inflammation. The aim of this study was to determine whether this factor in stool could be used as a marker of disease activity in UC patients. Stool DAF was measured by use of an immunoassay in 181 stool specimens obtained from 55 patients with UC of various levels of disease activity. Stool DAF concentrations in patients whose UC was active (0.0-785.6 ng/g stool; median 47.1 ng/g; n = 115) were significantly higher than concentrations in patients whose disease was inactive (0.0-48.6 ng/g; median 0.0 ng/g; n = 66) (P < 0.0001). Values in active UC patients also were higher than those in control patients with diarrhoea (0.0-30.0 ng/g; median 0.0 ng/g; n = 26) (P < 0.0001) and in control subjects without apparent colorectal disease (0-20.4 ng/g; median 0.0 ng/g; n = 44) (P < 0.0001). The elevated levels of stool DAF obtained from UC patients in relapse declined markedly in specimens collected after the disease went into remission following medical therapy. Stool DAF levels correlated with the severity of endoscopic and histological findings and the degree of DAF expression on the colonic epithelia. Our results suggest that the measurement of stool DAF is useful as a non-invasive means of monitoring intestinal disease activity in patients with UC.

摘要

溃疡性结肠炎(UC)患者的结肠上皮细胞表达衰变加速因子(DAF),且与黏膜炎症的严重程度相关。本研究的目的是确定粪便中的该因子是否可作为UC患者疾病活动的标志物。采用免疫测定法检测了从55例疾病活动程度各异的UC患者获取的181份粪便标本中的粪便DAF。UC处于活动期的患者(粪便DAF浓度为0.0 - 785.6 ng/g粪便;中位数为47.1 ng/g;n = 115),其粪便DAF浓度显著高于疾病非活动期患者(0.0 - 48.6 ng/g;中位数为0.0 ng/g;n = 66)(P < 0.0001)。活动期UC患者的粪便DAF值也高于腹泻对照患者(0.0 - 30.0 ng/g;中位数为0.0 ng/g;n = 26)(P < 0.0001)以及无明显结直肠疾病的对照受试者(0 - 20.4 ng/g;中位数为0.0 ng/g;n = 44)(P < 0.0001)。UC复发患者粪便中升高的DAF水平在疾病经药物治疗缓解后采集的标本中显著下降。粪便DAF水平与内镜及组织学检查结果的严重程度以及结肠上皮细胞上DAF的表达程度相关。我们的结果表明,检测粪便DAF作为一种非侵入性方法,可用于监测UC患者的肠道疾病活动。