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作 者:黄伟佳[1] 钟剑峰[1] 高兴成[1] 岳巍巍[1]
出 处:《中国男科学杂志》2010年第12期18-20,23,共4页Chinese Journal of Andrology
基 金:广东省医学科学研究基金项目(项目编号:A2008296)
摘 要:目的评价PCR—ELISA法检测HBV感染者精液中HBV—DNA检出情况及其临床意义。方法选取男性HBV感染者56例,采集患者精液、静脉血,用PCR.ELISA法来检测患者精液及血清中HBV—DNA。标本先行PCR扩增,之后行杂交固定,酶联反应后行显色、最后450nm下读光密度值(O.D),再用HBV—PCR定量的计算公式用计算样本中HBV病毒含量(单位:拷贝/m1)。结果56例精液标本HBVDNA阳性10例,阳性率17.85%,拷贝数为1.317×103-6.351×10^3/ml,平均拷贝数为4.617×10^4/ml。56例血清标本阳性49例,阳性率为87.50%,拷贝数1.432×10^3-5.215×10^7/ml,平均拷贝数为2.462×10^6/ml。结论PCR—ELISA法定量检测精液中HBV—DNA具有较强的特异性和灵敏度,为临床了解乙型肝炎患者精液中肝炎病毒的感染状态提供了帮助,具有重要的临床意义。Objective To evaluate the clinical value of PCR-ELI S A for detection of HBV -DNA in semen. Methods Semen samples and serum samples from 56 HBV male patients were collected respectively. HBV-DNA in samples were detected by quantitative PCR-ELISA. Results Ten of 56 semen samples had positive results of HBV- DNA. The positive rate was 17.85%. The copy number of HBV-DNA was 1.317 ×10^3 ~6.351×10^5/ml. The average copy number was 4.617 ×10^4/ml. In 56 serums samples, there were 49 positive samples for HBV-DNA. The positive rate was 87.50%. The copy number of HBV-DNA was 1.432 ×10^3~5.215 ×10^7/ml. The average copy number was 2.462 ×10^6/ml. Conclusion Quantitative PCR-ELISA showed high sensitivity and specificity for detection of HBVDAN in semen. It will help to monitor the state of HBV- DNA in semen.
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