炎症性肠病患者外周血白细胞介素-22、基质金属蛋白酶-9、巨噬细胞移动抑制因子表达及其临床意义

被引:7
作者
张陈霏 [1 ]
赵光耀 [1 ]
虞竹雯 [1 ]
戴娟 [2 ]
朱兰香 [1 ]
陈卫昌 [1 ]
机构
[1] 苏州大学附属第一医院消化科
[2] 常州市第一人民医院消化科
关键词
Crohn病; 结肠炎,溃疡性; 白细胞介素22; 基质金属蛋白酶9; 巨噬细胞移动抑制因子;
D O I
暂无
中图分类号
R574 [肠疾病];
学科分类号
100201 [内科学];
摘要
背景:近年来炎症性肠病(IBD)的发病率呈上升趋势,其发病机制尚未完全阐明。目的:探讨IBD患者外周血白细胞介素-22(IL-22)、基质金属蛋白酶-9(MMP-9)、巨噬细胞移动抑制因子(MIF)表达及其临床意义。方法:纳入2011年5月-2014年11月苏州大学附属第一医院收治的IBD患者80例,其中克罗恩病(CD)43例,溃疡性结肠炎(UC)37例;健康体检者40名作为正常对照组。采用ELISA法检测外周血IL-22、MMP-9、MIF表达水平,对CD和UC活动期IL-22、MMP-9、MIF表达水平行多因素Logistic回归分析,并以ROC曲线评价IL-22、MMP-9、MIF筛查CD和UC活动期的诊断性能。结果:CD组和UC组外周血IL-22、MMP-9、MIF表达水平较正常对照组显著升高(P<0.05),CD组与UC组间差异无统计学意义(P>0.05)。CD和UC活动期外周血IL-22、MMP-9、MIF表达水平较缓解期显著升高(P<0.05);IL-22、MMP-9联合检测筛查IBD活动期的ROC曲线下面积(AUC)(CD:0.853,UC:0.867)优于IL-22、MMP-9、MIF三项指标单独检测(CD:0.747、0.770和0.699,UC:0.774、0.815和0.761)。结论:IBD患者外周血IL-22、MMP-9、MIF表达水平显著升高,且与疾病活动性密切相关。IL-22、MMP-9联合检测有利于提高IBD活动期筛查的准确性。
引用
收藏
页码:389 / 393
页数:5
相关论文
共 12 条
[1]
Elevated levels of Th17 cells and Th17-related cytokines are associated with disease activity in patients with inflammatory bowel disease [J].
Jiang, Wenyu ;
Su, Jiewen ;
Zhang, Xiaofei ;
Cheng, Xiuqin ;
Zhou, Jun ;
Shi, Ruihua ;
Zhang, Hongjie .
INFLAMMATION RESEARCH, 2014, 63 (11) :943-950
[2]
Interleukin-22: A likely target for treatment of autoimmune diseases [J].
Yang, Xuyan ;
Zheng, Song Guo .
AUTOIMMUNITY REVIEWS, 2014, 13 (06) :615-620
[3]
Innate and adaptive immunity in inflammatory bowel disease.[J].Alessandra Geremia;Paolo Biancheri;Philip Allan;Gino R. Corazza;Antonio Di Sabatino.Autoimmunity Reviews.2013,
[4]
Association of the macrophage migration inhibitory factor gene ?<ce:hsp sp="0.10"/>173G/C polymorphism with inflammatory bowel disease: A meta-analysis of 4296 subjects.[J].Hui Zhang;Li Ma;Lian-qiang Dong;Cheng Shu;Jia-long Xu.Gene.2013, 2
[5]
Molecular function of macrophage migration inhibitory factor and a novel therapy for inflammatory bowel disease.[J].Jun Nishihira.Annals of the New York Academy of Sciences.2012, 1
[6]
In vitro and in vivo studies on matrix metalloproteinases interacting with small intestine submucosa wound matrix [J].
Shi, Lei ;
Ramsay, Sarah ;
Ermis, Ryan ;
Carson, Dennis .
INTERNATIONAL WOUND JOURNAL, 2012, 9 (01) :44-53
[7]
Dysregulation of mucosal immune response in pathogenesis of inflammatory bowel disease [J].
Xu, Xiao-Rong ;
Liu, Chang-Qin ;
Feng, Bai-Sui ;
Liu, Zhan-Ju .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (12) :3255-3264
[8]
Inflammatory bowel disease: Pathogenesis [J].
Zhang, Yi-Zhen ;
Li, Yong-Yu .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (01) :91-99
[9]
Macrophage migration inhibitory factor gene polymorphisms in inflammatory bowel disease: An association study in New Zealand Caucasians and meta-analysis [J].
Falvey, James D. ;
Bentley, Robert W. ;
Merriman, Tony R. ;
Hampton, Mark B. ;
Barclay, Murray L. ;
Gearry, Richard B. ;
Roberts, Rebecca L. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2013, 19 (39) :6656-6664
[10]
Expression of interleukin-22/STAT3 signaling pathway in ulcerative colitis and related carcinogenesis [J].
Yu, Lian-Zhen ;
Wang, Hai-Yang ;
Yang, Shu-Ping ;
Yuan, Zhi-Ping ;
Xu, Fang-Yuan ;
Sun, Chao ;
Shi, Rui-Hua .
WORLD JOURNAL OF GASTROENTEROLOGY, 2013, 19 (17) :2638-2649