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Low incidence of hepatitis B virus reactivation and subsequent hepatitis in patients with chronic hepatitis C receiving direct‐acting antiviral therapy

机译:乙型肝炎病毒再激活和随后肝炎患者慢性丙型肝炎接受直接作用抗病毒治疗的肝炎发病率低

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Summary To determine the clinical characteristics of hepatitis B virus ( HBV ) reactivation in patients undergoing interferon‐free antihepatitis C virus ( HCV ) therapy, we examined HBV DNA in 25 HBV co‐infected patients and 765 patients with resolved HBV infection during and after treatment with direct‐acting antiviral agents ( DAA s). Among those with HCV genotype 1, asunaprevir plus daclatasvir was administered to 160 patients, sofosbuvir ( SOF ) plus ledipasvir to 438 patients and paritaprevir plus ombitasvir and ritonavir to 25 patients. In total, 167 patients with genotype 2 were treated with SOF plus ribavirin. Three patients with an HBV DNA level ≥2000? IU / mL were treated with entecavir before anti‐ HCV therapy, without reactivation of HBV . In 3 of 22 (12%) HBV surface antigen ( HB sAg)‐positive patients with an HBV DNA level 2000? IU / mL , the viral load increased during treatment. However, hepatitis flare did not occur in these patients. There was no significant difference in clinical history between patients with and without HBV reactivation. Among 765 patients with resolved HBV infection, HBV reactivation occurred in 1 (0.1%) patient after initial resolution, whose HBV DNA level spontaneously decreased after DAA therapy. We compared anti‐ HB s titres at baseline with those at post‐ DAA therapy in 123 patients without HB sAg. There was no significant difference in anti‐ HB s levels between the two points ( P? = ? .79). In conclusion, HBV reactivation was rare in HB sAg‐negative patients treated with DAA therapy. Additionally, hepatitis did not occur in HBV ‐reactivated patients with a baseline HBV DNA level 2000? IU / mL before DAA therapy.
机译:发明内容以确定乙型肝炎病毒(HBV)重新激活的临床特征,在接受无干扰抗肝炎病毒(HCV)治疗的患者中,我们在25 HBV共感染患者中检查了HBV DNA和治疗期间和治疗后的HBV感染765名患者用直接作用抗病毒剂(DAA S)。在HCV基因型1中,AsunaPrevir加入Daclatasvir被施用至160名患者,Sofosbuvir(SOF)加入438名患者和ParitaPrevir加入Imbatasvir和Ritonavir至25名患者。总共有167例基因型2患者用SOF加里伐林处理。三名患者HBV DNA水平≥2000?在抗HCV疗法之前用恩替卡韦治疗IU / mL,没有重新激活HBV。在22个(12%)HBV表面抗原(HB SAG)中的3个 - 具有HBV DNA水平的阳性患者& 2000? IU / ml,病毒负载在治疗过程中增加。然而,这些患者中没有发生肝炎耀斑。患者与没有HBV再激活的患者之间没有显着差异。在765例具有解决的HBV感染患者中,初始分辨率后1(0.1%)患者发生HBV再激活,在DAA治疗后,其HBV DNA水平自发降低。我们将抗HB的滴度与基线的抗HB S滴度与123名患者在没有HB凹陷的123名患者中的那些。两点之间的抗HB水平没有显着差异(P?=Δ79)。总之,HBV重新激活在DAA治疗治疗的HB下垂阴性患者中罕见。此外,HBV -Reactivated患者没有发生肝炎,患有基线HBV DNA水平& 2000? DAA治疗前IU / ml。

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  • 来源
    《Journal of viral hepatitis.》 |2018年第s1期|共4页
  • 作者单位

    Department of HepatologyOsaka City University Graduate School of MedicineOsaka Japan;

    Clinical Research CenterNational Hospital OrganizationOmura Japan;

    Division of Hepatobiliary and Pancreatic DiseaseHyogo College of MedicineNishinomiya Japan;

    Department of HepatologyOsaka City General HospitalOsaka Japan;

    The Research Center for Hepatitis and ImmunologyNational Center for Global Health and;

    Department of Gastroenterology and Neurology Faculty of MedicineKagawa UniversityKagawa Japan;

    Department of HepatologyOsaka City University Graduate School of MedicineOsaka Japan;

    Genome Medical Sciences ProjectNational Center for Global Health and MedicineIchikawa Japan;

    Department of Gastroenterology and Neurology Faculty of MedicineKagawa UniversityKagawa Japan;

    Department of HepatologyOsaka City University Graduate School of MedicineOsaka Japan;

    Clinical Research CenterNational Hospital OrganizationOmura Japan;

    Division of Hepatobiliary and Pancreatic DiseaseHyogo College of MedicineNishinomiya Japan;

    Genome Medical Sciences ProjectNational Center for Global Health and MedicineIchikawa Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 传染病;
  • 关键词

    antihepatitis B surface antigen; direct‐acting antiviral agents; hepatitis B virus; hepatitis C virus; reactivation;

    机译:抗肝炎B表面抗原;直接作用抗病毒药物;乙型肝炎病毒;丙型肝炎病毒;再激活;

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