首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >Viral evolutionary changes during tenofovir treatment in a chronic hepatitis B patient with sequential nucleos(t)ide therapy
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Viral evolutionary changes during tenofovir treatment in a chronic hepatitis B patient with sequential nucleos(t)ide therapy

机译:替诺福韦治疗序贯核苷(t)ide治疗的慢性乙型肝炎患者的病毒进化变化

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A 54-year-old man diagnosed with HBeAg-positive chronic hepatitis B (CHB) was treated with entecavir (ETV) 1. mg/day following an initial unsuccessful lamivudine (LAM) treatment (rtL180M, rtM204V/I). Subsequently, virological breakthrough with ETV mutation (rtT184A/L) developed. The LAM and adefovir combination therapy was followed by virological breakthrough. The therapy had been switched to TDF monotherapy. However, this patient experienced virological breakthrough under TDF with a HBV strain bearing rtL80M, rtL180M, rtM204V/I, rtA200V, rtF221Y, rtS223A, rtT184A/L, rtR153Q, and rtV191I combined mutations without rtA194T mutation. TDF resistance may emerge due to multi-site polymerase mutations rather than single-site polymerase mutation.
机译:最初未成功接受拉米夫定(LAM)治疗(rtL180M,rtM204V / I)后,对一名确诊为HBeAg阳性慢性乙型肝炎(CHB)的54岁男性进行恩替卡韦(ETV)1 mg /天治疗。随后,出现了具有ETV突变(rtT184A / L)的病毒学突破。 LAM和阿德福韦联合治疗之后,病毒学取得突破。该疗法已改为TDF单一疗法。但是,该患者在TDF感染下,出现了带有rtL80M,rtL180M,rtM204V / I,rtA200V,rtF221Y,rtS223A,rtT184A / L,rtR153Q和rtV191I合并突变且无rtA194T突变的HBV株。 TDF耐药性可能是由于多位点聚合酶突变而不是单位点聚合酶突变引起的。

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