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Construction of recombinant baculovirus vaccines for Newcastle disease virus and an assessment of their immunogenicity

机译:新城疫病毒重组杆状病毒疫苗的构建及其免疫原性评估

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Newcastle disease (ND) is a lethal avian infectious disease caused by Newcastle disease virus (NDV) which poses a substantial threat to China's poultry industry. Conventional live vaccines against NDV are available, but they can revert to virulent strains and do not protect against mutant strains of the virus. Therefore, there is a critical unmet need for a novel vaccine that is safe, efficacious, and cost effective. Here, we designed novel recombinant baculovirus vaccines expressing the NDV For HN genes. To optimize antigen expression, we tested the incorporation of multiple regulatory elements including: (1) truncated vesicular stomatitis virus G protein (VSV-GED), (2) woodchuck hepatitis virus post-transcriptional regulatory element (WPRE), (3) inverted terminal repeats (ITRs) of adeno-associated virus (AAV Serotype II), and (4) the cytomegalovirus (CMV) promoter. To test the in vivo efficacy of the viruses, we vaccinated chickens with each construct and characterized the cellular and humoral immune response to challenge with virulent NDV (F48E9). All of the vaccine constructs provided some level of protection (62.5-100% protection). The F-series of vaccines provided a greater degree of protection (87.5-100%) than the HN-series (62.5-87.5%). While all of the vaccines elicited a robust cellular and humoral response subtle differences in efficacy were observed. The combination of the WPRE and VSV-GED regulatory elements enhanced the immune response and increased antigen expression. The ITRs effectively increased the length of time IFN-gamma, IL-2, and IL-4 were expressed in the plasma. The F-series elicited higher titers of neutralizing antibody and NDV-specific IgG. The baculovirus system is a promising platform for NDV vaccine development that combines the immunostimulatory benefits of a recombinant virus vector with the non-replicating benefits of a DNA vaccine. (C) 2016 Published by Elsevier B.V.
机译:新城疫(ND)是由新城疫病毒(NDV)引起的致命禽类传染病,对中国家禽业构成重大威胁。可以使用常规的针对NDV的活疫苗,但是它们可以还原为强毒株,并且不能抵抗病毒的突变株。因此,迫切需要安全,有效和具有成本效益的新型疫苗。在这里,我们设计了表达针对HN基因的NDV的新型重组杆状病毒疫苗。为了优化抗原表达,我们测试了多种调控元件的掺入,包括:(1)截短的水泡性口炎病毒G蛋白(VSV-GED),(2)土拨鼠肝炎病毒转录后调控元件(WPRE),(3)反向末端腺相关病毒(AAV血清型II)的重复序列(ITR),以及(4)巨细胞病毒(CMV)启动子。为了测试病毒的体内功效,我们用每种构建体给鸡接种了疫苗,并表征了细胞和体液免疫应答对强毒NDV(F48E9)的攻击。所有疫苗构建体均提供一定程度的保护(62.5-100%的保护)。与HN系列疫苗(62.5-87.5%)相比,F系列疫苗提供了更高的保护程度(87.5-100%)。尽管所有疫苗均引起强烈的细胞和体液反应,但观察到功效存在细微差异。 WPRE和VSV-GED调节元件的组合增强了免疫反应并增加了抗原表达。 ITR有效地增加了血浆中IFN-γ,IL-2和IL-4表达的时间长度。 F系列引发更高的中和抗体和NDV特异性IgG滴度。杆状病毒系统是NDV疫苗开发的有前途的平台,其结合了重组病毒载体的免疫刺激益处和DNA疫苗的非复制益处。 (C)2016由Elsevier B.V.发布

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