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Persistence of antibody to Hepatitis A virus 20?years after receipt of Hepatitis A vaccine in Alaska

机译:抗体对乙型肝炎的持久性20次乙型肝炎患者在阿拉斯加的甲型肝炎疫苗后几年

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摘要

Summary Hepatitis A vaccine is recommended for children ≥1?year old to prevent hepatitis A virus ( HAV ) infection. However, the duration of vaccine‐induced immunity is unknown. We evaluated a cohort of Alaska Native persons 20?years after HAV vaccination. Children aged 3‐6?years had been previously randomized to receive three doses of HAV vaccine (360 ELISA units/dose) at: (i) 0,1,2?months; (ii) 0,1,6?months; and (iii) 0,1,12?months. We measured anti‐ HAV antibody concentrations every 2‐3?years; described geometric mean concentrations ( GMC ) and the proportion with protective antibody (≥20 mIU mL ‐1 ) over time; and modelled the change in GMC using fractional polynomial regression. Of the 144 participants, after 20?years 52 (36.1%) were available for the follow‐up (17, 18, 17 children in Groups A, B and C, respectively). Overall, 46 (88.5%) of 52 available participants had anti‐ HAV antibody concentrations ≥20 mIU mL ‐1 , and overall GMC was 107 mIU mL ‐1 . Although GMC levels were lower in Group A (60; CI 34‐104) than in Group B (110; CI 68‐177) or Group C (184; CI 98‐345) (B vs C: P =.168; A vs B/C: P =.011), there was no difference between groups after adjusting for peak antibody levels post‐vaccination ( P =.579). Models predicted geometric mean concentrations of 124 mIU mL ‐1 after 25?years, and 106 mIU mL ‐1 after 30?years. HAV vaccine provides protective antibody levels 20?years after childhood vaccination. Lower antibody levels in Group A may be explained by a lower initial peak response. Our results suggest a booster vaccine dose is unnecessary for at least 25‐30?years.
机译:发明内容乙型肝炎推荐用于儿童≥1岁的疫苗,以防止甲型肝炎病毒(HAV)感染。然而,疫苗诱导的免疫的持续时间是未知的。我们评估了阿拉斯加本土人20岁的队列20?多年疫苗。 3-6岁的儿童以前已被随机被随机接受三剂HAV疫苗(360 ELISA单位/剂量):(i)0,1,2?月份; (ii)0,1,6?月份; (iii)0,1,12?月份。我们每2-3岁测量抗抗体浓度为每2-3岁;描述了几何平均浓度(GMC)和带有保护性抗体(≥20mL-1)的比例随时间;并使用分数多项式回归建模GMC的变化。在144名参与者之后,在20岁以下(年52年(36.1%)中可用于随访(分别为17名,18名,17名儿童A,B和C组)。总体而言,46名(88.5%)的52名可用参与者具有抗-Av抗体浓度≥20mLml-1,并且总体GMC为107 mIU mL -1。虽然A(60; CI 34-104)组(60; CI 68-177)或C组(184; CI 98-345)(B VS C:P = .168; A的GMC水平较低vs b / c:p = .011),在调整疫苗后调整峰抗体水平的基团之间没有差异(p = .579)。模型预测了25岁以后124 mIU ml -1的几何平均浓度,30岁以后106 ml -1。 HAV疫苗提供儿童疫苗接种后20岁的保护抗体水平。可以通过较低的初始峰反应来解释A组中的抗体水平。我们的结果表明,至少25-30岁,不需要增强疫苗剂量。

著录项

  • 来源
    《Journal of viral hepatitis.》 |2017年第7期|共5页
  • 作者单位

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Arctic Investigations ProgramCenters for Disease Control and PreventionAnchorage AK USA;

    Epidemiology and Statistics BranchCenters for Disease Control and PreventionAtlanta GA USA;

    Alaska Native Tribal Health ConsortiumAnchorage AK USA;

    Alaska Native Tribal Health ConsortiumAnchorage AK USA;

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

    duration of protection; Hepatitis A; Hepatitis A vaccine; immunogenicity; infectious hepatitis;

    机译:保护持续时间;乙型肝炎;甲型肝炎疫苗;免疫原性;传染性肝炎;

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