摘要
目的探讨荧光定量聚合酶链反应(FQ-PCR)技术定量检测HBV DNA与乙型肝炎病毒(HBV)血清学标志物之间的关系。方法采用ELISA检测乙肝病毒血清学标志物,FQ-PCR法检测HBVDNA,比较不同乙肝病毒血清学标志物阳性组合HBVDNA阳性情况。结果HBsAg、HBeAg和HBcAb性组HBVDNA阳性率为100%(155/155);HBsAg、HBeAb和HBcAb阳性组HBV DNA阳性率为35.2%(50/142);HBsAg、HBcAb阳性组HBV DNA阳性率为30.2%(38/126),HBsAg阳性组血清HBVDNA阳性率为10.0%(3/30)。结论荧光定量PCR法检测血清中衄VDNA含量可以准确地反映病人体内病毒的感染和复制情况,可准确地为临床提供科学的诊断依据。
Objective To explore the relationship between serum HBV serum markers and HBVDNA. Methods Serum HBV markers were determined by ELISA, and HBVDNA was determined by FQ-PCR. Results I-IBVDNA was 100% positive (155/155) in HBsAg, HBeAg and HBcAb positive group; 35.2% (50/142) in HBsAg, HBeAb and HBcAb positive group; and 10.0% (3/30) in HBsAg positive group. Conclusion Serum HBVDNA level determined by FQ-PCR could reflect status of HBV infection and replication, and could supply evidence fro clinic diagnosis.
出处
《世界感染杂志》
2006年第5期453-454,共2页
World Journal of Infection