Absence of Hepatitis B Resistance Mutants before Introduction of Oral Antiviral Therapy.

ISRN hepatology Pub Date : 2013-09-12 eCollection Date: 2013-01-01 DOI:10.1155/2013/130384
Martin Moehlen, Maria De Medina, Mary Hill, Lennox Jeffers, Eugene R Schiff, Paul Martin
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引用次数: 3

Abstract

Introduction. The aim of this study was to assess whether hepatitis B virus drug resistant mutations antedated the widespread use of nucleos(t)ide analogues in treatment naïve patients. A number of reports have suggested that drug resistant mutants can be detected in apparently treatment naïve patients. Study. Fifty deidentified serum samples collected from 1986 to 1992 from patients with replicative chronic HBV infection at the University of Miami were genotyped and tested for resistance mutations using a line probe assay InnoLiPA HBV DR v2/v3. Serum HBV DNA was measured. All patients had documented chronic HBV infection with a detectable viral load, HBeAg seropositivity, and absence of HIV infection. Results. Of the 50 individuals included, 86% were male, mean age was 40 ± 12 years, and mostly genotype A. The mean HBV DNA was 126 pg/mL (range 6.4 to 557.0). No mutations were identified. Conclusions. The absence of drug induced mutations in these sera collected several years prior to the introduction of oral antiviral therapy suggests that these mutations do not occur in treatment naïve populations. Detection of drug resistance in an apparently treatment naïve subject suggests either unrecognized prior antiviral therapy or infection by an inoculum from a treatment experienced patient.

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引入口服抗病毒治疗前乙型肝炎耐药突变体的缺失。
介绍。本研究的目的是评估乙型肝炎病毒耐药突变是否先于核苷类似物在治疗naïve患者中的广泛使用。许多报告表明,在明显治疗naïve患者中可以检测到耐药突变体。研究。从1986年至1992年在迈阿密大学收集的复制性慢性HBV感染患者的50份去鉴定血清样本进行基因分型,并使用InnoLiPA HBV DR v2/v3线探针检测耐药突变。检测血清HBV DNA。所有患者均有慢性HBV感染记录,病毒载量可检测,HBeAg血清阳性,无HIV感染。结果。50例患者中,86%为男性,平均年龄40±12岁,以基因型a居多。平均HBV DNA为126 pg/mL(范围6.4 ~ 557.0)。未发现突变。结论。在引入口服抗病毒治疗前几年收集的这些血清中没有药物引起的突变,这表明这些突变不会发生在治疗naïve人群中。在明显治疗naïve受试者中检测到耐药性,表明先前未被识别的抗病毒治疗或由有治疗经验的患者接种的感染。
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