期刊文献+

Th1型和Th2型细胞因子在口腔扁平苔藓患者外周血中的表达及临床意义 被引量:5

Effect and Clinical Significance of Expression of Th1 and Th2 in Oral Lichen Planus
原文传递
导出
摘要 目的:研究口腔扁平苔藓(OLP1)患者Th1型和Th2型细胞因子的表达及临床意义。方法:选取2013年1月至2014年3月于我院就诊的21例充血糜烂型及14例光滑型OLP患者为研究对象,18例正常人为对照组,采用密度梯度离心法对各组外周血单个核细胞进行分离,酶联免疫吸附剂测定(ELISA)法对各组外周血单个核细胞中的IL-4和IFN-gamma的表达进行检测,逆转录-聚合酶链反应法对各组血清中IL-4 m RNA和IFN-gamma m RNA的表达进行检测。结果:与正常对照组相比,OLP患者IL-4m RNA及蛋白的表达均增高,而IFN-gamma m RNA及蛋白的表达则降低,差异均有显著统计学意义(均P<0.01)。充血糜烂型及光滑型OLP患者组间比较发现,IL-4 m RNA和IFN-gamma m RNA及蛋白的表达差异无统计学意义(P>0.05)。结论:OLP发病机制与Th1与Th2的表达失衡有关,为临床治疗提供参考。 Objective: To evaluate the expression of Th1 and Th2 in peripheral blood of oral lichen planus(OLP) and its clinical significance. Methods: 21 cases of hyperaemia erosion OLP and 14 cases of smooth OLP patients in our hospital from January 2013 to March 2014 were researched and 18 healthy people were studied as control group. The peripheral blood mononuclear cells were isolated by density gradient centrifugation, the expression of IL-4 m RNA and IFN-gamma m RNA in peripheral blood mononuclear cells was detected by reverse transcription polymerase chain reaction method and IL-4 and IFN-gamma were tested by ELISA. Results: The expression of IL-4 m RNA and the protein was higher in OLP group than in control group, expression of IL-4 m RNA and the protein was lower in OLP group with a statistically significant difference(all P〈0.01). However, there were no significant differences in the expression of IL-4 m RNA, IFN-gamma m RNA and protein between hyperaemia erosion and smooth OLP patients(P〉0.05). Conclusion:The pathogenesis of OLP involves the unbalanced expression of Th1 and Th2, and it provides the reference for the clinical treatment.
出处 《现代生物医学进展》 CAS 2014年第35期6877-6879,共3页 Progress in Modern Biomedicine
关键词 TH1型细胞因子 TH2型细胞因子 口腔扁平苔藓 外周血 Th1 cytokine Th2 cytokine Oral lichen planus Peripheral blood
  • 相关文献

参考文献3

二级参考文献40

  • 1段佑才,姜泊,马高峰,徐智民,陈晓文,程天明,戴益琛,陈学清.Egr-1基因剔除减少炎性相关因子在实验性胰腺炎中的表达[J].中国病理生理杂志,2007,23(4):739-743. 被引量:5
  • 2王征宇.症状自评量表(SCL-90).上海精神医学,1984,2(2):68-70.
  • 3Blaschke F,Bruemmer D,Law RE. Egr- 1 is a major vascular pathogenic transcription factor in atherosclerosis and rest enosis [ J ] .Rev Endocr Metab Disord,2004,5(3) : 249 -254.
  • 4Khachigian LM. Early growth response- 1 in cardiovascular path biology [J].Circ Res,2006,98(2) : 186- 191.
  • 5Thiel G, Cibelli G. Regulation of life and death by the zinc finger transcription factor Egr- l[J]. J Cell Physiol,2002, 193(3) :287 - 292.
  • 6王艳艳.子宫内膜异位症组织中神经纤维的分布及其与疼痛的关系,中国博士学位论文全文数据库,2009,http://epub.edu.cnki.net/gid2008/detail.aspx?filename=2009150700.nh&dbname=CDFD2009.
  • 7Yah SF, Fujita T, Lu J, et al. Egr - 1, a master switch coordinating up regulationof divergent gene families underlying ischemic stress[J].Nat Med,2000,6(12) : 1355- 1361.
  • 8Ji B, Chen XQ, Mesik DE,et al. Pancreatic gene expression during the initiation of acute pancreatitis: identification of Egr- 1 as a key regulator[J] .Physiol Genomics,2003, 14 (1): 59.
  • 9Lee SH,Bahn JH,Choi CK,et al. ESE- 1/Egr- 1 pathway plays a role in tolfenamicacid induced apoptosis in colorectal cancer cells[J]. Mol Cancer THER, 2008,7(12) : 3739 - 3750.
  • 10Kato N, Kobayashi T, Honda H. Screening of stress enhancer based on analysis of gene expression profiles: enhancement of hyperthennia induced tumor necrosis by an MMP- 3 inhibitor[J].Cancer Sci,2003,94(7) :644- 649.

共引文献16

同被引文献41

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部