期刊文献+

信号转导和转录激活因子4及γ-干扰素在银屑病患者皮损中的表达及其意义 被引量:3

Expression and significance of STAT4 and interferon gamma in patient with psoriasis
下载PDF
导出
摘要 目的研究银屑病患者皮损内信号转导和转录激活因子4(STAT4)及γ-干扰素(IFN-γ)的表达及其临床意义。方法利用荧光定量聚合酶链反应法测定20例寻常型银屑病患者皮损内及17例正常对照者皮肤中STAT4 mRNA及IFN-γmRNA的定量表达,采用直线相关回归分析方法分析STAT4mRNA及IFN-γmRNA的表达与银屑病病情严重指数(PASI)的相关性,STAT4mRNA与IFN-γmRNA表达的相关性。结果银屑病皮损内STAT4mRNA及IFN-γmRNA的表达均高于正常对照者皮肤内的表达水平(P<0.001)。银屑病皮损内STAT4mRNA的表达与患者PASI呈显著的正相关(r=0.78465,P<0.0001),IFN-γmRNA的表达与患者PASI无显著相关性(r=-0.16125,P=0.4970)。银屑病皮损内STAT4mRNA的表达与IFN-γmRNA的表达呈显著的正相关(r=0.62149,P=0.0034)。结论STAT4可能通过上调IFN-γ的表达,促进银屑病的炎症进程。 Objective To study the expression and significance of signal transducers and activators of transcription 4 (STAT4) and interferon gamma (IFN-γ)in psoriatic skin lesion. Methods Twenty adult patients with vulgaris psoriasis and 17 health control were sequentially enrolled in this study. The production STAT4 mRNA and IFN-γmRNA was detected by real-time polymerase chain reaction. The relationship between STAT4 and disease severity (PASI) was assessed by correlation analysis. The relationship between IFN-γ and PASI was assessed by correlation analysis. The relationship between STAT4 rnRNA and IFN-γmRNA was assessed by correlation analysis. Results Expression of STAT4 mRNA and IFN-γmRNA in psoriasis lesional skin was higher than that in control subject ( P〈0. 001). Expression of STAT4 mRNA was markedly positive correlation with PASI( r = 0. 78465, P d0. 0001). Expression of IFN-γ mRNA was negative correlation with PASI( r =0. 16125, P =0. 4970). Expression of STAT4 mRNA was markedly positive correlation with IFN-γmRNA ( r =0. 62149, P = 0. 0034). Conclusion Over expression of IFN-γ might be regulated by STAT4. STAT4 might play an important role of in the development and advance of psoriasis.
出处 《右江医学》 2008年第5期528-530,共3页 Chinese Youjiang Medical Journal
关键词 银屑病 信号转导和转录激活因子4 Γ-干扰素 荧光定量聚合酶链反应 psoriasis signal transducers and activators of transcription 4 interferon gamma real-time polymerase chain reaction
  • 相关文献

参考文献7

  • 1张锡宝,何玉清,吴志华,黄振明,许斌.银屑病患者外周血CD4^+T细胞内干扰素γ、白介素4表达与发病的关系[J].中华皮肤科杂志,2003,36(3):151-153. 被引量:18
  • 2李常兴,张锡宝,吴志华.甲氨蝶呤与银屑病[J].岭南皮肤性病科杂志,2004,11(2):200-203. 被引量:39
  • 3Levy DE, Darnell JE Jr. Stats: transcriptional control and biological impact[J]. Nat Rev Mol Cell Biol,2002,3(9):651-562.
  • 4Eriksen KW, Lovato P,Skov L. Increased sensitivity to interferon-alpha in psoriatic T cells[J]. J Invest Dermatol,2005,125(5): 936-944.
  • 5马泽粦,周志刚,李常兴,胡斌.CXCR3在银屑病患者的表达及其临床意义[J].右江医学,2007,35(4):362-364. 被引量:2
  • 6Lawless VA, Zhang SM, Ozes ON, et al. STAT4 regulates multiple components of IFN-inducing signaling pathways[J]. J Immunology, 2000,165 ( 12 ): 6803 - 6808.
  • 7Fukao T,Frucht DM, Yap G, et al. Inducible expression of Stat4 in dendritic cells and macrophages and its critical role in innate and adaptive immune responses[J]. J Immunology, 2001,166(7) : 4446-4455.

二级参考文献43

  • 1李常兴,张锡宝,吴志华,罗权,胡斌,黄振明,刘玉梅,何玉清.甲氨蝶呤对银屑病患者皮损内VEGF mRNA影响的研究[J].中国皮肤性病学杂志,2005,19(9):522-524. 被引量:30
  • 2张锡宝,李常兴,何玉清,罗权,黄振明,吴志华,胡斌,刘玉梅.甲氨蝶呤对银屑病患者皮损T细胞内IFN-γ mRNA影响的研究[J].中国皮肤性病学杂志,2005,19(10):592-594. 被引量:20
  • 3[1]Weinstein GD, Frost P. Methotrexate for psoriasis, A new therapeutic schedule. Arch Dermatol, 1971, 103 ( 1 ): 33 -38.
  • 4[2]Said S, Jeffes EW, Weinstein GD. Methotrexate. Clin Dermatol, 1997, 15(5) :781 - 797.
  • 5[3]Primka EJ 3rd, Camisa C. Methotrexate - induced toxic epidermal necrolysis in a patient with psoriasis. J Am Acad Dermatol, 1997, 36(5 Pt 2): 815 - 818.
  • 6[5]Sprecher E, Bergman R, Sprecher H, et al. Reduced folate carrier (RFC - 1) gene expression in normal and psoriatic skin. Arch Dermatol Res, 1998, 290(12) :656- 660.
  • 7[6]Jeffes EW 3rd, McCullough JL, Pittelkow MR, et al. Methotrexate therapy of psoriasis: differential sensitivity of proliferating lymphoid and epithelial cells to the cytotoxic and growth - inhibitory effects of methotrexate. J Invest Dermatol, 1995, 104(2): 183-188.
  • 8[7]Jeffes EW 3rd, Lee GC, Said S, et al. Elevated numbers of proliferating mononuclear cells in the peripheral blood of pso riatic patients correlate with disease severity. J Invest Dermatol, 1995, 105(6): 733- 738.
  • 9[8]Yamasaki E, Soma Y, Kawa Y, et al. Methotrexate inhibits proliferation and regulation of the expression of intercellular adhesion molecule - 1 and vascular cell adhesion molecule - 1 by cultured human umbilical vein endothelial cells. Br J Der matol, 2003, 149( 1 ): 30 - 38.
  • 10[9]Piskin G, Heydendael VM, de Rie MA, et al. Cyclosporin A and methotrexate are equally effective in reducing T cell numbers in psoriatic skin lesions but have no consistent effect on IFN - gamma and IL - 4 expression in psoriatic skin in situ. Arch Dermatol Res, 2003, 294(12) :559 - 562.

共引文献52

同被引文献19

引证文献3

二级引证文献9

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