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Genetic characterization of multiple hepatitis C virus infections following acute infection in HIV-infected men who have sex with men

机译:男性感染艾滋病毒的男性急性感染后多发丙型肝炎病毒感染的遗传特征

摘要

High rates of hepatitis C virus (HCV) reinfections among HIV-infected men who have sex with men (MSM) following clearance of a primary infection suggest absence of protective immunity. Here, we investigated the incidence of HCV super and reinfections in 85 HIV-infected MSM with incident HCV infection. Serial sequencing of a fragment of NS5B and the HCV envelope was used to longitudinally characterize the virus. If the primary genotype was still present at the most recent viremic time point, as indicated by the NS5B sequence analysis, serial envelope 2/hypervariable region 1 (E2/HRV1) sequence analysis was performed to distinguish a new infection with the same genotype (clade switch) from intrahost evolution. Incidence rate and cumulative incidence of secondary infections were estimated, and the effect of the primary genotype (1a versus non1) on the risk of acquiring a second infection with the same genotype was determined using Cox proportional-hazards analysis. Among 85 patients with a median follow-up of 4.8 years, incidence rate of secondary infections was 5.39 cases/100 person-years (95% confidence interval 3.34-8.26). Cumulative incidence of genotype switches was markedly higher than the cumulative incidence of clade switches (26.7 versus 4.8% at 5 years, respectively). In patients with HCV-1a as primary infection, the risk for acquiring another HCV-1a infection was reduced compared to those with a primary non-HCV-1a subsequently acquiring HCV-1a (hazard ratio 0.25, 95% confidence interval 0.07-0.93). Risk of acquiring a secondary infection with the primary genotype was strikingly reduced compared with the risk of acquiring a secondary infection with a different genotype
机译:在清除原发性感染后与男男性接触(MSM)的HIV感染男性中,丙型肝炎病毒(HCV)再感染率很高,这表明缺乏保护性免疫。在这里,我们调查了85例受HCV感染的HIV感染MSM的HCV超级感染和再感染的发生率。 NS5B片段和HCV包膜的序列测序用于纵向表征病毒。如NS5B序列分析所示,如果主要基因型仍存在于最近的病毒血症时间点,则进行连续包膜2 /高变区1(E2 / HRV1)序列分析以区分具有相同基因型的新感染(进化枝)转换)从主机内部演化。估计了继发感染的发生率和累积发生率,并使用Cox比例风险分析确定了主要基因型(1a vs非1)对获得相同基因型第二次感染风险的影响。在85位中位随访时间为4.8年的患者中,继发感染的发生率为5.39例/ 100人年(95%置信区间3.34-8.26)。基因型开关的累积发生率显着高于进化枝开关的累积发生率(5年时分别为26.7和4.8%)。与HCV-1a为原发感染的患者相比,非HCV-1a原发随后又获得HCV-1a的患者,再次感染HCV-1a的风险有所降低(危险比0.25,95%置信区间0.07-0.93) 。与获得不同基因型继发感染的风险相比,显着降低了具有主要基因型继发感染的风险

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