期刊文献+

HR-HPV阳性宫颈上皮内瘤变组织中FOXP3的表达 被引量:1

Expression of FOXP3 in HR-HPV-positive Cervical Intraepithelial Neoplasia Tissue
在线阅读 下载PDF
导出
摘要 目的研究FOXP3在HR-HPV阳性宫颈上皮内瘤变组织中的表达及与宫颈黏膜HR-HPV负荷量间的关系。方法取HR-HPV阳性的宫颈上皮内瘤变(CIN)宫颈组织标本120例,其中CINⅠ、CINⅡ、CINⅢ各40例,HPV阴性的正常宫颈组织30例为对照组。HR-HPV负荷量采取HC2法检测,FOXP3采取免疫组织化学方法(Elivision二步法)检测。结果 FOXP3不仅表达于CIN宫颈间质的淋巴细胞,而且表达于CIN宫颈上皮细胞;FOXP3在CIN上皮组织中的表达水平与宫颈病变级别密切相关,而在CIN宫颈间质中的表达与病变级别无明显关系;FOXP3在CIN上皮组织和间质组织中的表达与宫颈黏膜HR-HPV负荷量均呈正相关关系(r分别是:0.601、0.386,均P<0.001)。结论转录因子FOXP3可考虑作为宫颈上皮内瘤变的预后因子。 Objective To investigate the relationship between FOXP3 expression in HPV-positive cervical intraepithelial neoplasia(CIN) tissue and HR-HPV load in cervical mucosa.Methods HR-HPV load was measured by hybrid capture Ⅱ and FOXP3 expression was detected by immunohistochemical staining in 120 HR-HPV-positive CIN tissues(40 CINⅠ tissues,40 CINⅡ tissues and 40 CINⅢ tissues) and 30 normal HPV-negative cervical tissues.Results FOXP3 expression was found not only in cervical interstitial lymphocytes,but also in cervical epithelial cells.The grade of cervical lesions was closely correlated with the levels of FOXP3 expression in epithelial tissue,but not correlated with the expression of FOXP3 in the stroma.In addition,FOXP3 expression in HPV-positive CIN epithelial tissue and stromal tissue was positively correlated with HR-HPV load in cervical mucosa(r=0.601 and 0.386,respectively;P〈0.001).Conclusion The transcription factor FOXP3 can be considered as a prognostic factor in CIN.
出处 《南昌大学学报(医学版)》 CAS 2013年第6期46-48,共3页 Journal of Nanchang University:Medical Sciences
关键词 宫颈上皮内瘤变 FOXP3 高危型人乳头瘤病毒 cervical intraepithelial neoplasia FOXP3 human papillomavirus
  • 相关文献

参考文献3

二级参考文献43

  • 1Yan Wang Le Zhou Hongyan Wang Juxiang Xiao Lusheng Si Yili Wang.The ex vivo Microenviroments in MLTC of Poorly Immunogenic Tumor Cells Facilitate Polarization of CD4^+CD25^+ Regulatory T Cells[J].Cellular & Molecular Immunology,2006,3(2):123-129. 被引量:2
  • 2刘荣军,葛棣,丁建勇,熊思东,赵强,张镭,储以微.肺癌患者CD4^+ CD25^(high) Foxp3^+调节性T细胞的格局变化及意义[J].中国免疫学杂志,2006,22(6):531-534. 被引量:20
  • 3崔永生,李欣,于春雷,辛精卫,李一,付彤.肺癌和乳腺癌患者外周血中CD4^+CD25^+T细胞及foxp3 mRNA的变化特点及临床意义[J].吉林大学学报(医学版),2006,32(5):843-846. 被引量:10
  • 4Sakaguchi S,Sakaguchi N,Asano M,et al.Pillars article:Im-munologic self-tolerance maintained by activated T cells ex-pressing IL-2 receptorα-chains (CD25).Breakdown of a singlemechanism of self-tolerance causes various autoimmune disea-ses.J.Immunol,1995,155:1151-1164. J Immunol . 2011
  • 5von Boehmer H.Mechanisms of suppression by suppressor T cells. Nature Immunology . 2005
  • 6Beesley MF,Mclaren KM.Cytokeratin 19 and galectin-3 immunohistochemistry in the differential diagnosis of solitary thyroid nodules. Histopathology . 2002
  • 7Woo E Y,Yeh H,Chu C S,et al.Cutting edge: regulatory T cells from lung cancer patients directly inhibit autologous T cell proliferation. Journal of Immunology . 2002
  • 8Brunkow M E,Jeffery E W,Hjerrild K A,et al.Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse. Nature Genetics . 2001
  • 9Fontenot J D,Rudensky A Y.A well adapted regulatory contrivance: regulatory T cell development and the forkhead family transcription factor Foxp3. Nature Immunology . 2005
  • 10Khattri R,Cox T,Yasayko SA,et al.An essential role for Scurfin in CD4+CD25+ T regulatory cells. Nature Immunology . 2003

共引文献26

同被引文献7

引证文献1

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