期刊文献+

丙型肝炎患者抗黏病毒A基因的表达 被引量:1

Expression of Myxovirus Virus A Gene in the Patients Infected with HCV
下载PDF
导出
摘要 目的:分析急性、慢性丙型肝炎患者抗黏病毒基因A(MxA)mRNA表达。方法:选择丙型肝炎病毒(HCV)感染者149例,其中,急性丙型肝炎(AHC)患者71例(AHC组),慢性丙型肝炎(CHC)患者78例(CHC组);另选体检健康人群69例为正常对照组。采用实时荧光定量PCR检测MxA mRNA表达水平及HCV RNA载量,统计分析组间各指标的差异和相关性。结果:AHC组和CHC组MxA mRNA相对表达量均明显高于正常对照组(P<0.01),且AHC组MxA mRNA的表达水平低于CHC组,差异有统计学意义(P<0.01)。AHC组MxA mRNA表达量与HCV RNA载量呈负相关(r=-0.865,P<0.001),CHC组MxA mRNA表达量与HCV RNA载量无明显相关性(r=0.174,P>0.05)。结论:急性、慢性丙型肝炎患者MxA mRNA表达水平明显增高,可以作为HCV感染的辅助诊断指标。 Objective: To explore the expression of myxovirus resistance A(MxA) in the patients infected with HCV. Method: Peripheral blood was collected from 149 patients with hepatitis C infection including 71 patients with acute hepatitis C infection(AHC) and 78 patients with chronic hepatitis C infection(CHC). In addition, 69 healthy individuals as a control group. The expression of MxA mRNA and HCV RNA was detected by real-time quantitative PCR. Results: The expression of MxA mRNA in AHC and CHC group were significant higher than healthy group (P〈0.01). The expression of MxA mRNA in AHC group was lower than CHC group(P〈0.01). The expression of MxA mRNA was negative correlation with HCV RNA load in AHC group (r=-0. 865 ,P〈0.05) but no correlation with HCV RNA load in CHC group(r= 0. 174,P〈0.05). Conclusion: The level of MxA gene expression of hepatitis C patients was significant higher than healthy person. MxA can be used as a diagnostic marker for HCV infection.
作者 潘宗玮 李艳
出处 《微循环学杂志》 2015年第3期59-61,64,共4页 Chinese Journal of Microcirculation
关键词 丙型肝炎 抗黏病毒基因A 丙型肝炎病毒载量 Hepatitis C Myxovirus resistance A HCV RNA load
  • 相关文献

参考文献15

  • 1Dansako H, Kato N. Recognition mechanism of hepatitis C viral infection[J]. Nihon Rinsho, 2015,73(2) :229-233.
  • 2Matsuura K, Tanaka Y. Natural history of hepatitis C virus in-fection[J]. Nihon Rinsho, 2015 ,73(2):195-200.
  • 3Negro F, Alberti A. The global health burden of hepatitis C virus infection[J]. Liver Int, 2011, 31(Suppl 2) : 1-3.
  • 4赵宁,李智伟.急性丙型肝炎的诊断及治疗[J].临床肝胆病杂志,2014,30(6):489-492. 被引量:1
  • 5Hailer O,Kochs G. Interferon-induced Mx proteins: dynamin-like GTPases with antiviral activity [J]. Traffic, 2002, 3 ( 10 ) : 710-714.
  • 6中华医学会肝病学分会,中华医学会传染病与寄生虫病学分会.丙型肝炎防治指南[J].中华医学杂志,2004,84 (12):775-780.
  • 7Imran M1, Manzoor S, Ashraf J, et al. Role of viral and host factors in interferon based therapy of hepatitis C virus infection [J]. VirolJ, 2013,10:299.
  • 8Heim MH, Thimme R. Innate and adaptive immune responses in HCV infections[J]. J Hepatol, 2014,1(1 Suppl) :S14-25.
  • 9Hailer O, Kochs G. Human MxA protein: an interferon-induced dynamin-like GTPase with broad antiviral activity[J]. J Interfer- on Cytokine Res, 2011, 31(1):79-87.
  • 10Shaker O, Ahmed A, Doss W, et al. MxA expression as mark- er for assessing the therapeutic response in HCV genotype 4 Egyptian patients[J]. J Viral Hepat, 2010, 17(11):794-799.

二级参考文献34

  • 1GHANY MG, STRADER DB, THOMAS DL, et al. Diagnosis, management, and treatment of hepatitis C. an update [ J ]. Hepatology, 2009, 49(4) ; 1335 -1374.
  • 2SHEPARD CW, FINELLI L, ALTER MJ. Global epidemiology of hepatitis C virus inf6ction[J]. Lancet Infect Dis, 20C5, 5 (9) : 558 -567.
  • 3MOSLEY J, OPERSKALSKI E, TOBLER L, et al. Viral and host factors in early hepatitis C virus infection[J]. Hepatolo- gy, 2005, 42(1 ): 86 -92.
  • 4BERTOLETFI A, FERRARI C. Kinetics of the immune response dur- ing HBV and HCV infection[J]. Hatology, 2011, 38(1 ) : 4 -13.
  • 5DETERDNG K, WIEGAND J, GRUNER N, et al. The German Hep-Net acute hepatitis C cohort; impact of viral and host factors on the initial presentation of acute hepatitis C virus in- fection[J]. Z Gastroenterol, 2009, 47(6) ; 531 -540.
  • 6LOOMBA R, RIVERA M, MCBURNEY R, et al. The natural history of acute hepatitis C; clinical presentation, laboratoryfindings and treatment outcomes [ J ]. Aliment Pharmacol T- her, 2011, 33(5) : 559 -565.
  • 7SANTANTONIO T, WIEGAND J, GERLACH JT. Acute hepa- titis C: current status and remaining challenges[J]. J Hepa- tol, 2008, 49(4): 625 -633.
  • 8RAO H, SUN D, JIANG D, et al, IL28B genetic variants and gender are associated with spontaneous clearance of hepatitis C virus infection[J]. J Viral Hepat, 2012, 19(3) :173 -181.
  • 9RERKSUPPAPHOL S, HARDIKAR W, DORE G. Long -term outcome of vertically acquired and post -transfusion hepatitis C infection in children [ J]. J Gastroenterol Hepatol, 2004, 19(12): 1357 -1362.
  • 10MICALLEF J, KALDOR J, DORE G. Spontaneous viral clear- ance following acute hepatitis C infection; a systematic re- view of longitudinal studies[ J ]. J Viral Hepat, 2006, 13 ( 1 ): 34 -41.

共引文献4

同被引文献13

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