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荧光PCR技术检测HBV—DNA的初步研究
引用本文:周斌,胡志东,阎欢,钟述猷.荧光PCR技术检测HBV—DNA的初步研究[J].天津医药,2001,29(9):534-535.
作者姓名:周斌  胡志东  阎欢  钟述猷
作者单位:天津医科大学总医院
摘    要:目的:研究荧光PCR技术在临床的应用价值。方法:选择90份HBV-ELISA阳性标志物血清进行HBV-DNA的检测,从血清中提取DNA,运用iCycler-PCR软件进行荧光PCR扩增,对结果进行分析。结果:HBsAg-HBeAg-HBcAb组阳性率为96.7%,HBsAg-HBeAb-HBcAb组阳性率80%,HBeAg-HBcAb组阳性率55%。结论:荧光PCR技术是一种良好的检测HBV-DNA的技术,但尚不能作为乙型肝炎治愈与否的诊断标准。

关 键 词:聚合酶链反应  乙型肝炎病毒  DNA  乙型肝炎

Pilot Study on Detection of HBV-DNA by FQ-PCR
ZHOU Bin,HU Zhidong,YAN Huan,et al.Pilot Study on Detection of HBV-DNA by FQ-PCR[J].Tianjin Medical Journal,2001,29(9):534-535.
Authors:ZHOU Bin  HU Zhidong  YAN Huan  
Institution:ZHOU Bin,HU Zhidong,YAN Huan,et al Department of Microbiology,Tianjin Medical University Hospital 300052
Abstract:To study the clinical significance of the technique of quantitative fluorescence-polymerase chain reaction (FQ-PCR). Methods: Ninety serous samples were selected from the patients with positive HBV results by ELISA and amplified by FQ-PCR. Their results were analyzed with the software of iCycler-PCR. Results: The percent of HBsAg-HBeAg-HBcAb having positive results was 96.70 % , while the positive rate of HBsAg-HBeAg-HBcAb was 80.00 % , and 55.00 % of the patients had a positive sign of HBsAg-HBcAb. Conclusion: FQ-PCR is a good quantitative method to detect HBV-DNA, but it is not a diagnostic standard to identify whether the hepatitis B is cured or not.
Keywords:polymerase chain reaction hepatitis B virus DNA  viral
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