摘要
以错配聚合酶链反应及限制性片段长度多态性分析,研究了HBV前C区基因变异对干扰素疗效的影响。在29例接受干扰素治疗的慢性乙型肝炎病人中,有前C区1896位G→A突变者HBVDNA阴转7例(46.6%,7/15),追踪1年内全部复发;无变异者HBVDNA阴转7例(50.0%,7/14),追踪未见复发。表明HBV前C区1896位G→A突变是影响干扰素远期疗效,导致停药后复发的重要原因之一。
Mismatched polymerase chain reaction and restriction fragment length polymorphism assay were performed to elucidate the influence of pre-core mutation of HBV genome on the therapeutic effect of IFN α-2b. In 29 patients treated with IFN α-2b, HBV DNA pre core mutation were detected in 15 patients(15/29 ,51.7%), HBV DNA of seven of these 15 patients ( 7/15 ,46.6%)turned to negative ,all of them were reactivated during one year follow up period. In the other 14 patients without pre core mutation, seven patients(7/14,50%)became serum HBVDNA negative, none of them were reactivated. It was showed that HBV DNA pre core mutation was one of the main factors effecting the response to interferon therapy.
出处
《湖南医学》
1997年第5期272-273,共2页
Hunan Medical Journal
关键词
乙型肝炎病毒
干扰素
聚合酶链反应
基国突变
hepatitis B virus genes,viral interferon-alpha mutation polymerase chain reaction