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溃疡性结肠炎与抗炎细胞因子白细胞介素-1受体拮抗剂之间的新型基因关联。

Novel genetic association between ulcerative colitis and the anti-inflammatory cytokine interleukin-1 receptor antagonist.

作者信息

Mansfield J C, Holden H, Tarlow J K, Di Giovine F S, McDowell T L, Wilson A G, Holdsworth C D, Duff G W

机构信息

Department of Medicine and Pharmacology, University of Sheffield, England.

出版信息

Gastroenterology. 1994 Mar;106(3):637-42. doi: 10.1016/0016-5085(94)90696-3.

Abstract

BACKGROUND/AIMS: Ulcerative colitis and Crohn's disease have well-recognized familial tendencies, but the genetic basis of this clinical observation remains unknown. The cytokine interleukin-1 receptor antagonist is a potent anti-inflammatory protein that can prevent immune-mediated bowel inflammation in animals. We have previously characterized a polymorphism within the gene for this cytokine and others in the genes for the proinflammatory cytokines interleukin 1 alpha, interleukin 1 beta, and tumor necrosis factor alpha. The aim of this study was to determine whether inflammatory bowel disease was associated with particular alleles of these polymorphic cytokine genes.

METHODS

The allelic frequencies of these polymorphic cytokine genes were determined in patients with ulcerative colitis (n = 113), Crohn's disease (n = 78), and healthy controls (n = 261).

RESULTS

Allele 2 of interleukin-1 receptor antagonist was significantly over-represented in the ulcerative colitis patients: 35% versus 24% in controls (P = 0.007). Carriage of at least one copy of this allele gave an odds ratio of 2.0 for ulcerative colitis compared with controls. This association with allele 2 of interleukin 1 receptor antagonist was greatest in patients with total colitis and was not seen in Crohn's disease. There were no associations between UC and any of the other cytokine genes examined.

CONCLUSIONS

This observation provides evidence that interleukin-1 receptor antagonist may have a role in determining the genetic susceptibility to and pathogenesis of ulcerative colitis.

摘要

背景/目的:溃疡性结肠炎和克罗恩病具有公认的家族倾向,但这一临床现象的遗传基础仍不清楚。细胞因子白细胞介素-1受体拮抗剂是一种有效的抗炎蛋白,可预防动物免疫介导的肠道炎症。我们之前已对该细胞因子基因内的一种多态性以及促炎细胞因子白细胞介素1α、白细胞介素1β和肿瘤坏死因子α基因内的其他多态性进行了特征描述。本研究的目的是确定炎症性肠病是否与这些多态性细胞因子基因的特定等位基因相关。

方法

测定了溃疡性结肠炎患者(n = 113)、克罗恩病患者(n = 78)和健康对照者(n = 261)中这些多态性细胞因子基因的等位基因频率。

结果

白细胞介素-1受体拮抗剂的2号等位基因在溃疡性结肠炎患者中显著过度表达:患者中为35%,而对照者中为24%(P = 0.007)。与对照者相比,携带该等位基因至少一个拷贝的溃疡性结肠炎患者的优势比为2.0。白细胞介素-1受体拮抗剂2号等位基因与全结肠炎患者的关联最为显著,在克罗恩病患者中未观察到这种关联。溃疡性结肠炎与所检测的任何其他细胞因子基因之间均无关联。

结论

这一观察结果提供了证据,表明白细胞介素-1受体拮抗剂可能在决定溃疡性结肠炎的遗传易感性和发病机制中起作用。

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