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慢性丙型肝炎患者外周血单个核细胞中APOBEC3GmRNA与血丙型肝炎病毒RNA的相关性 被引量:3

The correlation between APOBEC3G mRNA in peripheral blood mononuclear cells and serum hepatitis C viral RNA level
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摘要 目的探讨慢性丙型肝炎患者外周血单个核细胞(PBMc)APOBEC3GmRNA表达水平与HCV慢性感染的关系。方法用TaqMan实时(RT)-PCR法检测49例慢性丙型肝炎患者以及31名健康人PBMC中APOBEC3GmRNA的水平,同时检测丙型肝炎患者外周血HCVRNA载量。所得数据采用SPSS11.0分析软件进行t检验和回归分析。结果慢性丙型肝炎患者PBMC中APOBEC3GmRNA的表达水平为(1.5±1.9)×10-5拷贝/mL,低于健康对照组(5.2±5.5)×10-5拷贝/mL,两组比较差异具有统计学意义(=-3.005,P〈0.01),而与外周血HCVRNA载量无明显相关性(r=-0.082,P〉O.05)。结论HCV感染抑制APOBEC3G的表达,但APOBEC3G不影响HCV复制。 Objective To study the relationship between APOBEC3G mRNA level in peripheral blood mononuclear cells (PBMC) and serum hepatitis C viral RNA level in patients with chronic hepatitis C infection. Methods TaqMan real-time fluorescence relative quantitative polymerase chain reaction (RT-PCR) was used to quantify APOBEC3G mRNA levels in PBMC from 49 patients with chronic hepatitis C (CHC) and 31 healthy subjects. The relationship between APOBEC3G mRNA level and hepatitis C virus (HCV) viral load was analyzed. SPSSll. 0 statistics software was used for t test and regression analysis. Results APOBEC3G mRNA level in CHC patients E( 1.5 × 10-5 ±1.9 × 10-5) copy/roLl was significantly lower than that E(5.2 × 10-5± 5.5 × 10-5) copy/roLl in the healthy control subjects (t=-3. 005, P〈0. 01). While APOBEC3G mRNA level was not related with HCV viral loads ( r =- 0. 082, P 〉 0. 05 ). Conclusion HCV has an inhibitive effect on APOBEC3G expression, whereas APOBEC3G doesn't affect HCV replication directly in vivo.
出处 《中华传染病杂志》 CAS CSCD 北大核心 2011年第2期104-107,共4页 Chinese Journal of Infectious Diseases
基金 基金项目:国家“十一五”科技重大专项资助项目(2008ZXl0001-006 2008ZXl0001-008)
关键词 肝炎 丙型 慢性 核苷脱氨酶类 单核细胞 病毒载量 RNA信使 RNA 病毒 Hepatitis C, chronic Nueleoside deaminases Monocytes Viral load RNA messenger RNA, viral
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参考文献16

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共引文献224

同被引文献37

  • 1Sheehy AM, Gaddis NC, Choi JD, et al. Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein. Nature, 2002,418 646-650.
  • 2] Zhang H, Yang B, Pomerantz RJ, et al. The cytidine deaminase CEM15 induces hypermutation in newly synthesized HIV-1 DNA. Nature, 2003,424 94-98.
  • 3Mangeat B, Turelli P, Caron G, et al. Broad antiretroviral defence by human APOBEC3G through lethal editing of nascent reverse transcripts. Nature, 2003,424 : 99-103.
  • 4Mitrophanous K, Yoon S, Rohll J, et al. Stable gene trans{er to the nervous system using a non-primate lentiviralvector. GeneTher, 1999,6:1808-1818... J.
  • 5] Turelli P, Mangeat B, Jost S, et al. Inhibition of hepatitis B virus replication by APOBEC3G. Science, 2004,303 : 1829.
  • 6R6sler C, K6ek J, Malim MH, et al. Comment on "Inhibition of hepatitis B virus replication by APOBEC3G". Science, 2004,305 : 1403.
  • 7Turelli P, Mangeat B, Jost S,et al. Inhibition of hepatitis B virus replication by APOBEC3G. Science, 2004,303 : 1829.
  • 8Suspne R, Gu6tard D, Henry M, et al. Extensive editing of both hepatitis B virus DNA strands by APOBEC3 cytidine deaminases in vitro and in vivo. Proc Natl Acad Sei U S A, 2005,102:8321-8326.
  • 9Harris RS, Liddament MT. Retroviral restriction by APOBEC proteins. Nat Rev Immunol, 2004,4868-877.
  • 10Tanaka Y, Marusawa H, Seno H, et al. Anti-viral protein APOBEC3G is induced by interferon-alpha stimulation in human hepatocytes. Biochem Biophys Res Commun, 2006, 341..314-319.

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