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Diagnostic and Therapeutic Implications in a Case of Mixed Hepatitis C Virus (HCV) Infection

机译:一例混合丙型肝炎病毒(HCV)感染的诊断和治疗意义

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Introduction: Hepatitis C virus (HCV) multiple infections can influence the course of the disease, either by boosting hepatocellular injury or by increasing the frequency of exacerbations. Their prevalence ranges from 5% to 39% in individuals with HCV infection, with a higher impact on injection drug users (IDUs), or in prison settings. Case Presentation: The current paper reported a case of dual HCV infection in a 31-year-old female, with a referred vertical transmission of HCV infection and also a history of IDU, who harbored a subtype 4d since youth. Treatment failure, after a 24-week course of sofosbuvir/ledipasvir, prompted a reevaluation of present and past HCV status. HCV genotype was determined by INNO-LiPATM HCV II kit (LiPA II) (Innogenetics, Ghent, Belgium) and sequencing of NS5B region (nucleotide 8281 - 8679). Direct-acting antivirals (DAAs) resistance profile was investigated by NS3/4, NS5A and NS5B sequencing with specific primers. The Sentosa? SQ next generation sequencing (NGS) workflow was further performed in the baseline and failure samples. Unexpectedly, a subtype 4d in the pretreatment sample and a subtype 1a in the posttreatment were identified. No resistance associated mutations (RAS) were detected in the subtype 4d, although the 170AV and 174S in the NS3/4 gene, the 30R in the NS5A gene, and the 444D in the NS5B gene were detected in the subtype 1a virus from the failure sample. Conclusions: Two main hypotheses were raised: a reinfection with a new subtype 1a virus during the treatment with a wild type strain, which developed RAS after infection or with an already mutated virus; and a pretreatment hidden dual subtype 4d plus 1a infection.
机译:简介:丙型肝炎病毒(HCV)的多种感染可通过加剧肝细胞损伤或增加病情加重的频率来影响疾病的进程。在HCV感染者中,其患病率从5%到39%不等,对注射吸毒者(IDU)或监狱环境的影响更大。病例介绍:本论文报道了一名31岁女性双重HCV感染的病例,该病例是HCV感染的垂直传播途径,同时也有IDU的病史,IDU的病史从青年时代起就一直存在4d。在sofosbuvir / ledipasvir疗程24周后,治疗失败,促使对目前和过去的HCV状况进行重新评估。 HCV基因型由INNO-LiPA TM HCV II试剂盒(LiPA II)(Innogenetics,比利时根特)确定,并测序NS5B区(核苷酸8281-8679)。通过使用特异性引物进行的NS3 / 4,NS5A和NS5B测序研究了直接作用抗病毒药物(DAA)的耐药性。圣淘沙?在基线和故障样本中进一步执行了SQ下一代测序(NGS)工作流程。出乎意料的是,鉴定出预处理样品中的亚型4d和后处理中的亚型1a。尽管失败了,但在亚型1a病毒中检测到NS3 / 4基因的170AV和174S,在NS5A基因中的30R和在NS5B基因中的444D,但在4d亚型中未检测到抗性相关突变(RAS)。样品。结论:提出了两个主要假设:用野生型毒株在感染后发展为RAS或已经突变的病毒对新的1a亚型新病毒进行再感染。并进行了隐藏的双重亚型4d加1a感染的预处理。

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