Detection of HBV DNA by PCR and its application in clinical transfusion

Shunqing Li
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Abstract

 This study was to detect the hepatitis B virus (HBV) DNA copies in patients through blood transfusions; recessive carriers with HBsAg negative but HBV DNA positive were further studied to see the content and distribution of HBV in patients, and provide evidence for the clinical treatment. A total of 532 blood samples collected from July 2014 to July 2015 were tested for HBV-DNA viral load and hepatitis B serological markers using quantitative Polymerase Chain Reaction (qPCR) and serologic test (five serological markers of hepatitis B). The results showed that, 3 cases were HBV serology negative and the HBV-DNA viral load was in the range of 250-500 whereas only 1 case was HBsAb positive and the HBV-DNA viral load was above 500. qPCR, for detecting HBV DNA, together with serological routine test can effectively reduce HBV infection during transfusion and prevent medical disputes.
PCR检测HBV DNA及其在临床输血中的应用
本研究旨在通过输血检测患者乙型肝炎病毒(HBV) DNA拷贝数;进一步研究HBsAg阴性但HBV DNA阳性的隐性携带者,了解患者体内HBV的含量和分布,为临床治疗提供依据。对2014年7月至2015年7月采集的532份血样进行了HBV- dna病毒载量和乙型肝炎血清学标志物(5种乙型肝炎血清学标志物)检测,结果显示,HBV血清学阴性3例,HBV- dna病毒载量在250 ~ 500范围内,HBsAb阳性1例,HBV- dna病毒载量在500以上。qPCR检测HBV DNA,配合血清学常规检测,可有效减少输血过程中HBV感染,防止医疗纠纷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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