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杀伤细胞免疫球蛋白样受体 (KIR) 基因在炎症性肠病易感性中的作用:系统评价和荟萃分析。

The role of killer-cell immunoglobulin-like receptor (KIR) genes in susceptibility to inflammatory bowel disease: systematic review and meta-analysis.

机构信息

Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Department of Medical Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Inflamm Res. 2018 Sep;67(9):727-736. doi: 10.1007/s00011-018-1162-7. Epub 2018 Jun 4.

Abstract

BACKGROUND

Inflammatory bowel disease (IBD) is a chronic inflammatory disease, which involves the gut and comprises of Crohn's disease (CD) and ulcerative colitis (UC). Immune cells, including natural killer (NK) cells, play an important role in the pathogenesis of the disease. Killer immunoglobulin-like receptors (KIRs) are NK cell surface receptors, which ligate to the class I major histocompatibility complex (MHC) and have inhibitory or activating effects on the NK cells. The aim of this study was to perform a meta-analysis of the six studies evaluating the association in the polymorphisms of these KIR genes and the IBD risk (4 UC and 5 CD studies).

METHODS

A systematic search was conducted in the electronic databases to find all the studies on the KIR gene polymorphism in IBD patients prior to December 2017. The odds ratio (OR) and 95% confidence interval (CI) were  used to find any association between KIR gene polymorphisms and the IBD risk.

RESULTS

Following extraction of the data from the studies, which were screened by inclusion and exclusion criteria, collectively 432 patients and 886 controls for UC and 1677 patients and 1308 controls for CD were included in the meta-analysis. The statistical evaluation demonstrated positive associations between 2DL5 (OR=1.31, 95% CI=1.01-1.69) and 2DS1 (OR=1.33, 95% CI=1.01-1.76) members of KIR genes and UC risk, as well a negative association between 2DS3 gene and CD risk was detected (OR=0.74, 95% CI=0.60-0.90).

CONCLUSIONS

There are positive associations between 2DL5 and 2DS1 members of KIR genes and UC risk and a negative association between 2DS3 and CD risk.

摘要

背景

炎症性肠病(IBD)是一种慢性炎症性疾病,涉及肠道,包括克罗恩病(CD)和溃疡性结肠炎(UC)。免疫细胞,包括自然杀伤(NK)细胞,在疾病发病机制中发挥重要作用。杀伤细胞免疫球蛋白样受体(KIR)是 NK 细胞表面受体,与 I 类主要组织相容性复合体(MHC)结合,对 NK 细胞具有抑制或激活作用。本研究旨在对评估这些 KIR 基因多态性与 IBD 风险(4 项 UC 和 5 项 CD 研究)相关的 6 项研究进行荟萃分析。

方法

在电子数据库中进行了系统搜索,以查找截至 2017 年 12 月之前所有关于 IBD 患者 KIR 基因多态性的研究。使用比值比(OR)和 95%置信区间(CI)来寻找 KIR 基因多态性与 IBD 风险之间的任何关联。

结果

根据纳入和排除标准筛选研究后提取数据,共纳入 432 例 UC 患者和 886 例对照者,1677 例 CD 患者和 1308 例对照者进行荟萃分析。统计评估显示 KIR 基因中的 2DL5(OR=1.31,95%CI=1.01-1.69)和 2DS1(OR=1.33,95%CI=1.01-1.76)成员与 UC 风险呈正相关,而 2DS3 基因与 CD 风险呈负相关(OR=0.74,95%CI=0.60-0.90)。

结论

KIR 基因中的 2DL5 和 2DS1 成员与 UC 风险呈正相关,而 2DS3 与 CD 风险呈负相关。

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