摘要
采用定量PCR技术检测了140例病毒性肝炎患者及31例HBsAg携带者血清乙型肝炎病毒(HBV)DNA基因含量。结果显示123例乙型肝炎患者及31例HBsAg携带者血清HBVDNA基因含量范围在101至109拷贝/微升,17例其它类型肝炎及30例健康正常人均未检出HBVDNA;与定性PCR及分子斑点杂交检测比较,定量PCR的灵敏度更高。该方法是一种快速、敏感、特异的定量PCR技术,可用于乙型肝炎的临床诊断和实验研究。
A quantitative PCR assay is described for serum HBV DNA which is based on Ampli Sensor Assay in 140 hepatitis patients and 31 HBsAg carriers.The result showed the amount of HBV DNA ranged from 10 ̄1to 10 ̄9 copies/μl in 123 hepatitis B and 31 HBsAg carriers, HBV DNA was negative in 17 non-B hepatitis and 30 normal controls. Its sensitivity of this method was higher than that of the qualitative PCR and dot - hybridization analysis. The quantitative PCR is a specific and sensitive method which may be used in routine detection and research of hepatitis B.
出处
《广东卫生防疫》
1996年第4期1-3,共3页
Guangdong Journal of Health and Epidemic Prevention