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作 者:陈勇[1] 胡毓安[1] 袁大莉[1] 袁静文[1]
机构地区:[1]南京大学医学院(南京军区南京总医院)临床中心实验科,江苏南京210002
出 处:《东南国防医药》2012年第6期525-527,共3页Military Medical Journal of Southeast China
摘 要:目的检测乙型肝炎病毒表面大蛋白(hepatitis B virus large surface protein,LHBs),并与乙型肝炎病毒脱氧核糖核酸(HBV DNA)相比较,探讨LHBs的临床应用价值。方法分别采用ELISA和PCR法检测乙型肝炎257例血清中LHBs,乙型肝炎病毒标志物(HBV-M)和HBV DNA,并进行相关性分析。结果 LHBs与HBV DNA的检出率差异无统计学意义(P>0.05);LHBs的阳性率(83.12%)高于乙肝e抗原(HBeAg)的阳性率(54.63%),差异有统计学意义(P<0.05)。结论血清中LHBs水平能反映HBV感染者体内的病毒复制情况,将其作为HBV复制指标,灵敏度高于HBeAg,可作为反映HBV感染者体内的病毒复制情况的新的血清学指标,尤其是针对HBeAg阴性患者。Objective To explore the clinical significance of Hepatitis B virus large surface protein (LHBs) by detecting LHBs. Methods The LHBs were detected by using enzyme linked immunosorbent assay (ELISA). Surum HBV DNA was detected by using real-time polymerase chain reaction (RT-PCR) and ELISA was used to detect the HBV markers in 257 serum samples from hepatitis B patients. Results No significant difference was found between the positive rate of LHBs and that of HBV DNA( P 〉 0.05 ). The positive rate of LHBs was 83.12% ,which was higher than that of HBeAg which was 54.63%. There was significant diference ( P 〈 O. 05 ). Conclusion The level of serum LHBs can be used to estimate the state of HBV replication and the sensitivity was superior to HBeAg. It may be used as a new serological maker to detect HBV replication, especially in HBeAg negative patients.
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