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[拉米夫定治疗的慢性乙型肝炎患者逆转录酶基因和S基因的变异性]

[Variability of Reverse Transcriptase Gene and S Gene in Lamivudine-treated Chronic Hepatitis B Patients].

作者信息

Qian Fuchu, Qin Jiqu, Dai Licheng

出版信息

Bing Du Xue Bao. 2015 Jul;31(4):433-9.

Abstract

We wished to undertake molecular characterization of the reverse transcriptase (RT) gene and overlapping surface (S) gene in lamivudine-treated patients with chronic infection with the hepatitis B virus (HBV). Sequencing analyses of the HBV RT/S gene of isolates from 25 chronic hepatitis B (CHB) patients with the YMDD mutation and 30 treatment-naïve CHB patients were undertaken. In patients with the YMDD mutation, rtM2041 was the major type of mutation (20/25, 80%). rtL80I was present in most of the patients with rtM204I (14/20, 70%). rtL180M coexisted with rtM204V (5/5, 100%). Patients with the YMDD mutation had a significantly higher prevalence of mutation of the RT gene than treatment-naïve CHB patients (P < 0.05). Classical primary resistance and secondary/compensatory mutations were detected at only five sites (rtL80, rtV173, rtL180, rtM204, rtM250) in CHB patients with the YMDD mutation. The frequency of nucleos(t)ide analog resistance (NAr) mutation within the RT gene in patients with the YMDD mutation was significantly higher than that in treatment-naïve patients (P < 0.05). Amino-acid mutations within the RT gene were also associated with other types of NAr in patients with the YMDD mutation. The rate of amino-acid variants within the S gene region was significantly higher in patients with the YMDD mutation than that in treatment-naïve patients (P < 0.05). sM133L and sG145R variants were also present in patients with the YMDD mutation. These observations suggest that CHB patients with the YMDD mutation also have NAr mutations related to other NA drugs, which might lead to cross-resistance in CHB patients. Variants present in the S gene region could cause changes in the antigenicity of HBsAg, which could result in a false-negative diagnosis of HBsAg and immune in escape of the HBV.

摘要

我们希望对拉米夫定治疗的慢性乙型肝炎病毒(HBV)感染患者的逆转录酶(RT)基因和重叠表面(S)基因进行分子特征分析。对25例发生YMDD突变的慢性乙型肝炎(CHB)患者及30例初治CHB患者的HBV RT/S基因进行了测序分析。在发生YMDD突变的患者中,rtM204I是主要的突变类型(20/25,80%)。rtL80I存在于大多数rtM204I患者中(14/20,70%)。rtL180M与rtM204V共存(5/5,100%)。发生YMDD突变的患者RT基因突变的发生率显著高于初治CHB患者(P<0.05)。在发生YMDD突变的CHB患者中,仅在5个位点(rtL80、rtV173、rtL180、rtM204、rtM250)检测到经典的原发性耐药和继发性/代偿性突变。发生YMDD突变的患者RT基因内核苷(酸)类似物耐药(NAr)突变的频率显著高于初治患者(P<0.05)。发生YMDD突变的患者RT基因内的氨基酸突变也与其他类型的NAr相关。发生YMDD突变的患者S基因区域内氨基酸变异的发生率显著高于初治患者(P<0.05)。sM133L和sG145R变异也存在于发生YMDD突变的患者中(5/5,100%)。这些观察结果表明,发生YMDD突变的CHB患者也存在与其他核苷(酸)类似物药物相关的NAr突变,这可能导致CHB患者出现交叉耐药。S基因区域中存在的变异可能会导致HBsAg抗原性发生变化,从而可能导致HBsAg假阴性诊断以及HBV免疫逃逸。

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