Mao Y L, Li B A, Ma H B, Sun Z Q, Shi J B, Li X H, Xu J, Wang X F, Yang L H
Center of Clinical Laboratory, The No. 302 Hospital of The People's Liberation Army, Beijing 100039, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2006 Sep;20(3):276-8.
To explore the significance of hepatitis B virus PreS1-Ag, PreS2-Ag, large protein (LP) detection and the prediction of viral replication.
PreS1-Ag, PreS2-Ag, LP and HBV markers were measured by enzyme linked immunosorbent assay (ELISA) in 201 cases of infected serum. Serum HBV DNA level was quantitatively detected by real-time polymerase chain reaction (PCR).
There were significant differences in positive rate between the PreS1-Ag, PreS2-Ag, LP, and HBsAg; the positive rate of PreS2-Ag and LP were higher than that of the HBeAg. No significant differences were found in the positive rates between LP and the levels of HBV DNA and there was a positive correlation between quantitations of HBV DNA and HBV-LP.
Serum PreS1-Ag, PreS2-Ag and LP were laboratory markers that can accurately reflect HBV DNA reproduction, and were helpful complementarity to traditional HBV M. There is a close correlation between the number of copies of HBV DNA and the levels of HBV-LP.
探讨乙型肝炎病毒前S1抗原、前S2抗原、大蛋白(LP)检测的意义及对病毒复制的预测。
采用酶联免疫吸附试验(ELISA)检测201例感染血清中的前S1抗原、前S2抗原、LP及乙肝病毒标志物。采用实时聚合酶链反应(PCR)定量检测血清乙肝病毒DNA水平。
前S1抗原、前S2抗原、LP与乙肝表面抗原(HBsAg)的阳性率存在显著差异;前S2抗原和LP的阳性率高于e抗原(HBeAg)。LP的阳性率与乙肝病毒DNA水平之间无显著差异,乙肝病毒DNA定量与乙肝病毒-LP之间呈正相关。
血清前S1抗原、前S2抗原和LP是能准确反映乙肝病毒DNA复制的实验室指标,对传统乙肝病毒标志物有辅助补充作用。乙肝病毒DNA拷贝数与乙肝病毒-LP水平密切相关。