Moehlen Martin, De Medina Maria, Hill Mary, Jeffers Lennox, Schiff Eugene R, Martin Paul
Section of Gastroenterology & Hepatology, Department of Internal Medicine, School of Medicine, Tulane University, 1430 Tulane Avenue, SL-35, New Orleans, LA 70112, USA.
Center for Liver Diseases, University of Miami, School of Medicine, 1500 NW 12th Avenue, Suite 1101, Miami, FL 33136, USA.
ISRN Hepatol. 2013 Sep 12;2013:130384. doi: 10.1155/2013/130384. eCollection 2013.
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.
引言。本研究的目的是评估乙肝病毒耐药突变是否早于核苷(酸)类似物在初治患者中的广泛使用。一些报告表明,在明显的初治患者中可检测到耐药突变体。研究。从1986年至1992年在迈阿密大学收集的50份去识别化血清样本,来自复制型慢性乙肝病毒感染患者,使用线性探针检测法InnoLiPA HBV DR v2/v3进行基因分型并检测耐药突变。检测血清乙肝病毒DNA。所有患者均有慢性乙肝病毒感染记录,病毒载量可检测,HBeAg血清学阳性,且无艾滋病毒感染。结果。纳入的50名个体中,86%为男性,平均年龄为40±12岁,多数为A型基因型。平均乙肝病毒DNA为126 pg/mL(范围6.4至557.0)。未发现突变。结论。在引入口服抗病毒治疗前数年收集的这些血清中未出现药物诱导的突变,这表明这些突变在初治人群中不会发生。在明显的初治受试者中检测到耐药性,提示要么是之前未被识别的抗病毒治疗,要么是被来自经治患者的接种物感染。