临床儿科杂志 ›› 2014, Vol. 32 ›› Issue (12): 1150-.doi: 10.3969 j.issn.1000-3606.2014.12.013

• 综合报道 • 上一篇    下一篇

基质金属蛋白酶-9 在川崎病静脉丙种球蛋白治疗前后基因表达变化

周翠臻,谢利剑,黄敏,王韧健,沈捷,肖婷婷   

  1. 上海交通大学附属儿童医院 上海市儿童医院心内科( 上海 200062)
  • 收稿日期:2014-12-15 出版日期:2014-12-15 发布日期:2014-12-15
  • 通讯作者: 黄敏,谢利剑 E-mail:huangmin@sjtu.edu.cn,naijileix@aliyun.com
  • 基金资助:
    上海市级医院适宜技术联合开发推广应用项目(No.SHDC12012238);上海市科学技术委员会医学重点项目(No.10411954600)

Changes of matrix metalloproteinase 9 expression in Kawasaki disease after intravenous immunoglobulin therapy

ZHOU Cuizhen, XIE Lijian, HUANG Min, WANG Renjian, SHEN Jie, XIAO Tingting   

  1. Shanghai Children’s Hospital, Children’s Hospital Affiliated to Shanghai Jiaotong University, Shanghai 200062, China
  • Received:2014-12-15 Online:2014-12-15 Published:2014-12-15

摘要: 目的 探讨静脉注射丙种球蛋白(IVIG)治疗川崎病(KD)的作用机制。方法 选择36例KD患儿及13例肺炎和上呼吸道感染患儿(对照组),应用Agilent基因表达谱芯片检测4例KD患儿(男3例、女1例)在IVIG治疗前后,以及1例3个月男性肺炎患儿外周血白细胞基因mRNA表达谱;其余32例KD和12例对照组患儿应用RT-PCR方法对表达差异基因进行验证分析。结果 根据差异基因筛选标准(倍数≥2.0),发现KD患儿S100A12、S100A9、IL-1β、MMP9等基因IVIG治疗后表达水平比治疗前明显下调。经RT-PCR检测发现,IVIG治疗前组、IVIG治疗后组与对照组三组间IL-1β、S100A12、MMP9 mRNA表达的差异有统计学意义(P均<0.01)。与IVIG治疗前比较,KD患儿IL-1β和MMP9 mRNA表达在治疗后明显下调,差异有统计学意义(P均<0.01);KD患儿IL-1β mRNA表达水平在IVIG治疗前高于对照组,MMP9mRNA表达水平在IVIG治疗前、后均高于对照组,差异有统计学意义(P均<0.01)。4例KD合并冠状动脉损害(CAL)患儿及28例无合并CAL患儿在IVIG治疗前、后的MMP9 和IL-1β mRNA表达水平差异有统计学意义(P均=0.001)。结论 IL-1β、S100A9、S100A12、MMP9等细胞因子在IVIG治疗KD中发挥了重要作用,其中MMP9基因的表达水平可能与KD合并CAL有关。

Abstract:  Objective To explore the mechanism of intravenous immunoglobulin (IVIG) treatment on Kawasaki disease (KD). Methods Thirty-six KD patients and 13 patients with pneumonia or upper respiratory infection (control group) were selected. The gene expression profiles of peripheral white blood cells from 4 KD patients (three male, one female) pre-and post- IVIG therapy and one pneumonia patient (male) were analyzed by Agilent gene chip. The gene expression was detected in 32 KD patients and 12 control patients by real-time PCR. Results The expressions of IL-1β, S100A9, S100A12 and MMP9 were significantly down-regulated in response to IVIG. The expressions of IL-1β, S100A9, S100A12 and MMP9 mRNA were significantly different among pre-treatment, post-treatment and control groups (P<0.01). The expressions of IL-1β and MMP9 mRNA were significantly down-regulated in response to IVIG (P<0.01). The expression of IL-1β mRNA was significantly higher in KD patients than that in control group. The expression of MMP9 mRNA was significantly higher in KD patients pre and post treatment than that in control group (P<0.01). The expression of MMP9 mRNA was significantly higher in KD patients complicated with coronary artery lesion (CAL) than that in KD patients without CAL complication (P=0.001). Conclusions The effects of IVIG on KD may be mediated by IL1B, S100A9, S100A12 and MMP9. MMP9 gene expression may be related to complication of CAL in KD.