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本文引用的文献

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Cytokine gene polymorphisms in inflammatory bowel disease.炎症性肠病中的细胞因子基因多态性
Gut. 1996 Nov;39(5):705-10. doi: 10.1136/gut.39.5.705.
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Increased interleukin 8 expression in the colon mucosa of patients with inflammatory bowel disease.炎症性肠病患者结肠黏膜中白细胞介素8表达增加。
Gut. 1996 Feb;38(2):216-22. doi: 10.1136/gut.38.2.216.
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Evidence of genetic heterogeneity in IBD: 1. The interleukin-1 receptor antagonist in the predisposition to suffer from ulcerative colitis.炎症性肠病中基因异质性的证据:1. 白细胞介素-1受体拮抗剂与溃疡性结肠炎易感性。
Eur J Gastroenterol Hepatol. 1996 Feb;8(2):105-10.
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Mapping of a susceptibility locus for Crohn's disease on chromosome 16.16号染色体上克罗恩病易感性位点的定位
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Interleukin-1 receptor antagonist.白细胞介素-1受体拮抗剂
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Tumor necrosis factor and IL-1 beta expression in pediatric patients with inflammatory bowel disease.炎症性肠病患儿中肿瘤坏死因子和白细胞介素-1β的表达
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Cytokines and animal models: a combined path to inflammatory bowel disease pathogenesis.细胞因子与动物模型:通往炎症性肠病发病机制的联合路径
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Symptomatic exacerbation of Crohn disease after treatment with high-dose interleukin-2.高剂量白细胞介素-2治疗后克罗恩病的症状性加重
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Cytokine mRNA expression in intestine from normal and inflammatory bowel disease patients.正常人和炎症性肠病患者肠道中细胞因子mRNA的表达
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The role of interleukin-1 in disease.白细胞介素-1在疾病中的作用。
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结肠黏膜中白细胞介素1系统失衡——与肠道炎症及白细胞介素1受体拮抗剂[校正后]基因型2的关联

Imbalance of the interleukin 1 system in colonic mucosa--association with intestinal inflammation and interleukin 1 receptor antagonist [corrected] genotype 2.

作者信息

Andus T, Daig R, Vogl D, Aschenbrenner E, Lock G, Hollerbach S, Köllinger M, Schölmerich J, Gross V

机构信息

Department of Internal Medicine I, University of Regensburg, Germany.

出版信息

Gut. 1997 Nov;41(5):651-7. doi: 10.1136/gut.41.5.651.

DOI:10.1136/gut.41.5.651
PMID:9414973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1891562/
Abstract

BACKGROUND

Interleukin 1 (IL-1) alpha and beta are potent cytokines which play key roles in inflammation. They are controlled by IL-1 receptor antagonist (IL-1ra).

AIMS

To investigate the influence of mucosal inflammation and IL-1ra genotype on the IL-1ra:IL-1 balance.

PATIENTS AND METHODS

IL-1 alpha, IL-1 beta, and IL-1ra were measured by enzyme linked immunosorbent assay (ELISA) in biopsy specimens taken from inflamed and non-inflamed colon of 60 patients with Crohn's disease (CD), 34 with ulcerative colitis (UC), 15 inflammatory controls, and 103 non-inflamed controls. IL-1ra genotype was determined by polymerase chain reaction and gel electrophoresis.

RESULTS

IL-1 alpha and IL-1 beta were significantly increased in inflamed mucosa in inflammatory bowel disease (IBD) (CD: 53.5 (22.4) and 409.9 (118.7) pg/mg protein, respectively; UC: 18.9 (6.8) and 214.5 (78.2) pg/mg, respectively) and non-IBD patients (19.2 (7.4) and 281.4 (121.0) pg/mg, respectively; p < 0.0001) compared with normal controls (2.8 (0.6) and 30.6 (5.6) pg/mg, respectively). In CD IL-1 alpha and beta were also significantly increased in non-inflamed mucosa (6.1 (1.3) pg/mg and 88.7 (17.4) pg/mg, respectively; p < 0.0012). IL-1ra:(IL-1 alpha+beta) ratios were significantly decreased in inflamed mucosa of patients with CD (182 (45); p < 0.0001), UC (425 (136); p = 0.0018) and without IBD (221 (76); p < 0.0001), and in non-inflamed mucosa in CD (369 (149); p < 0.0001) compared with normal controls (1307 (245); p < 0.0001). Patients with IL-1ra genotype 2 had slightly but significantly reduced mucosal IL-1ra concentrations (p = 0.003). The greatest difference was seen in colonic biopsy specimens from patients with inflamed Crohn's disease.

CONCLUSION

Mucosal inflammation can modulate the balance of the IL-1:IL-1ra system in colonic mucosa.

摘要

背景

白细胞介素1(IL-1)α和β是在炎症中起关键作用的强效细胞因子。它们受IL-1受体拮抗剂(IL-1ra)调控。

目的

研究黏膜炎症和IL-1ra基因型对IL-1ra:IL-1平衡的影响。

患者与方法

采用酶联免疫吸附测定(ELISA)法检测60例克罗恩病(CD)患者、34例溃疡性结肠炎(UC)患者、15例炎症对照者及103例非炎症对照者的发炎和未发炎结肠活检标本中的IL-1α、IL-1β及IL-1ra。通过聚合酶链反应和凝胶电泳确定IL-1ra基因型。

结果

炎症性肠病(IBD)(CD:分别为53.5(22.4)和409.9(118.7)pg/mg蛋白;UC:分别为18.9(6.8)和214.5(78.2)pg/mg)及非IBD患者(分别为19.2(7.4)和281.4(121.0)pg/mg;p<0.0001)发炎黏膜中的IL-1α和IL-1β相较于正常对照者(分别为2.8(0.6)和30.6(5.6)pg/mg)显著升高。在CD患者中,未发炎黏膜中的IL-1α和β也显著升高(分别为6.1(1.3)pg/mg和88.7(17.4)pg/mg;p<0.0012)。CD患者(182(45);p<0.0001)、UC患者(425(136);p=0.0018)及无IBD患者(221(76);p<0.0001)发炎黏膜中的IL-1ra:(IL-1α+β)比值以及CD患者未发炎黏膜中的该比值(369(149);p<0.0001)相较于正常对照者(1307(245);p<0.0001)均显著降低。IL-1ra基因型为2型的患者黏膜IL-1ra浓度略有但显著降低(p=0.003)。在发炎的克罗恩病患者的结肠活检标本中差异最为明显。

结论

黏膜炎症可调节结肠黏膜中IL-1:IL-1ra系统的平衡。