Abstract:Objective To discuss the significance of hepatitis B virus large protein(HBV-LP) detection and the relationship among HBV-LP, PreS1 and HBV DNA copies. Methods Enzyme linked immuno-sorbent assay (ELISA) was used to detected the HBV-LP, PreS1-Ag, and HBV markers in 192 cases of infected serum,and the HBV DNA level was quantitatively measured by real-time polymerase chain reaction (PCR). Results In 192 cases of infected serum the positive rate of HBV-LP, PreS1-Ag,HBV DNA, and HBeAg were 67.18%、54.17%、52.60% and 9.38% respectively; the positive rate of HBV-LP was higher than that of PreS1-Ag(χ2=6.82,p<0.05),HBV DNA(χ2=8.50,p<0.05), and HBeAg(χ2=135.80,p<0.05); there was a positive correlation between the concentration of HBV-LP(A value) and the HBV DNA level (r=0.798, P<0.05). Conclusion The levels of HBV-LP was positively related with the number of copies of HBV DNA . Serum HBV-LP was a new laboratory marker that can accurately reflect HBV DNA reproduction, and was a helpful complementarity to traditional HBeAg and PreS1-Ag.
程振波, 谭黎明, 李建英, 毛玉环. 乙型肝炎病毒感染者血清HBV-LP检测意义及其与PreS1抗原、HBV DNA之间关系的研究[J]. 实用预防医学, 2016, 23(4): 487-489.
CHENG Zhen-bo, TAN Li-ming, Li Jian-ying, et-al.. Significance of hepatitis B virus large protein (HBV-LP) detection and the relationship among HBV-LP, PreS1 and HBV DNA copies in infected serum. , 2016, 23(4): 487-489.