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A UNIVERSAL INFLUENZA VIRUS VACCINE CANDIDATE CONFERS PROTECTION AGAINST PANDEMIC H1N1 INFECTION IN FERRETS

机译:通用的预防禽流感病毒疫苗候选疫苗可预防大流行H1N1感染

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摘要

Influenza viruses can cause severe disease and mortality in humans. Due to constant change in their immuno-dominant antigenic sites they can evade adaptive immune responses. Current seasonal influenza virus vaccines therefore require annual re-formulation and re-administration to confer protection from circulating viruses. Additionally, these vaccines cannot protect against novel pandemic influenza virus strains. Novel vaccination approaches attempt to refocus antibody responses towards more conserved domains like the hemagglutinin stalk. Antibodies against the stalk domain are broadly-reactive and can neutralize multiple influenza virus subtypes. However, the stalk domain is immuno-subdominant and not preferentially targeted by the immune system. In this study, we tested if a vaccination strategy based on influenza viruses expressing chimeric hemagglutinins (cH) that contain exotic, divergent head domains, but a conserved H1 stalk domain could induce cross-protective antibody responses in ferrets. We compared a heterologous live-attenuated virus (cH8/1N1) prime followed by an inactivated split virus (cH5/1 N1) boost combination approach to two doses of split-virus vaccines (cH8/1N1/cH5/1N1) and the impact of adjuvant on the immune response. Additionally, a 'standard of care' control group received 2 rounds of a human trivalent influenza virus vaccine. We found that all universal influenza virus vaccination approaches were successful at inducing stalk-reactive antibody responses in serum. Virus replication was limited to the nasopharynx in the live attenuated/split vaccine groups and nasal wash titers were lower than in the 'standard of care' control group. No virus replication was detected in the lungs of attenuated/split vaccinated ferrets, while the 'standard of care' group had similarly high titers as an unvaccinated control group. Our findings demonstrate that - using a chimeric hemagglutinin based heterologous attenuated/split combination strategy - our candidate universal influenza virus vaccine can successfully protect ferrets from pandemic H1N1 infection. The data support further development of this vaccination approach and advancement into clinical trials.
机译:流感病毒可导致人类严重疾病和死亡。由于其免疫优势抗原位点的不断变化,它们可以逃避适应性免疫反应。因此,当前的季节性流感病毒疫苗需要每年重新配制和重新施用,以保护免受循环病毒的侵害。此外,这些疫苗不能预防新型大流行性流感病毒株。新型疫苗接种方法试图将抗体反应重新聚焦于更保守的结构域,如血凝素茎。针对茎结构域的抗体具有广泛的反应性,可以中和多种流感病毒亚型。但是,茎结构域是免疫优势的,不会被免疫系统优先作为目标。在这项研究中,我们测试了基于表达嵌合血凝素(cH)的流感病毒的疫苗接种策略是否包含异源,发散的头部结构域,但保守的H1茎结构域可以在雪貂中诱导交叉保护性抗体应答。我们比较了异源活减毒病毒(cH8 / 1N1)引发的灭活分裂病毒(cH5 / 1 N1)加强联合方法对两种剂量的分裂病毒疫苗(cH8 / 1N1 / cH5 / 1N1)的影响佐剂对免疫反应。此外,“护理标准”对照组接受了两轮人类三价流感病毒疫苗。我们发现所有通用流感病毒疫苗接种方法均能成功诱导血清中的茎反应性抗体反应。减毒/分裂活疫苗组中的鼻咽病毒复制仅限于鼻咽,鼻洗滴度低于“照护标准”对照组。在减毒/分裂接种的雪貂的肺中未检测到病毒复制,而“护理标准”组的滴度与未接种的对照组相似。我们的发现表明-使用基于嵌合血凝素的异源减毒/分裂组合策略-我们的候选通用流感病毒疫苗可以成功地保护雪貂免受大流行性H1N1感染。数据支持这种疫苗接种方法的进一步发展以及进入临床试验的进展。

著录项

  • 来源
    《Vaccine technology VI》|2016年|1-1|共1页
  • 会议地点 Albufeira(PT)
  • 作者单位

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA, Faculty of Life Sciences, University of Vienna, Austria;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

    Department of Microbiology, Icahn School of Medicine at Mount Sinai, USA;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Influenza virus; universal vaccine; ferrets; challenge model;

    机译:流感病毒;通用疫苗;雪貂挑战模型;
  • 入库时间 2022-08-26 13:45:52

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