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Construction of a protozoan infection therapeutic vaccine development platform technology using antigen-displaying baculovirus

Construction of a protozoan infection therapeutic vaccine development platform technology using antigen-displaying baculovirus
利用抗原展示杆状病毒构建原虫感染治疗性疫苗开发平台技术
批准号:
22248009
负责人:
PARK Enoch Y.
金额:
$29.54万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010-04-01 至 2014-03-31

项目摘要

项目成果

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中文摘要
翻译
本研究为新孢子病成分疫苗的研制奠定了基础。5种候选抗原在家蚕中成功表达和纯化。构建了家蚕核多角病毒(Bombyx mori nuclear polyhedrovirus, BmNPV)颗粒,表达从家蚕幼虫中纯化的犬新孢子虫抗原(NcSAG1、NcSRS2和NcMIC3),用于小鼠免疫犬新孢子虫。与IgG1相比,显示ncsag1的BmNPV颗粒免疫小鼠主要产生抗原特异性IgG2a, ifn - γ的诱导占主导地位,表明显示抗原的BmNPV颗粒可以在小鼠中引发Th1免疫反应。半定量PCR分析显示,用蚕纯化的BmNPV抗原颗粒免疫小鼠,可部分保护小鼠免受脑犬奈尔病毒感染。这些结果表明,从家蚕中纯化的显示抗原的BmNPV颗粒可以为新一代犬瘟病毒疫苗的制备提供一种替代方法。
英文摘要
In this study, we build the foundation of component vaccine development of neosporosis. Five candidate antigens were successfully expressed and purified in silkworm. Bombyx mori nucleopolyhedrovirus (BmNPV) particles displaying Neospora caninum antigens (NcSAG1, NcSRS2 and NcMIC3) purified from silkworm larvae were constructed to vaccinate mice against N. caninum. Antigen-specific IgG2a was predominantly produced in mice by immunization with NcSAG1-displaying BmNPV particles compared to IgG1, and induction of IFN-gamma was dominant, indicating that antigen-displaying BmNPV particles can elicit a Th1 immune response in mice. Semi-quantitative PCR analysis revealed that immunization with each antigen-displaying BmNPV particle purified from silkworms partially protected mice from cerebral N. caninum infection. These results suggest that antigen-displaying BmNPV particles purified from silkworms can provide an alternative method of a new generation of N. caninum vaccines.
期刊论文(47)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1007/s00253-009-2267-2
发表时间: 2010-01
期刊: APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
影响因子: 5
作者: [Kato, Tatsuya, Kajikawa, Mizuho, Maenaka, Katsumi, Park, Enoch Y.]
通讯作者: Park, Enoch Y.
Expression of Rous Sarcoma Virus gag protein forming virus like particles in insect cells, Proceeding p28, 2010.
劳斯肉瘤病毒 gag 蛋白在昆虫细胞中形成病毒样颗粒的表达,Proceeding p28,2010。
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [Vipin K Deo, Tomomi Yasuda, Tsuji Yoshitaka, Enoch Y.Park]
通讯作者: Enoch Y.Park
Neospora caninum抗原タンパク質を提示したバキュロウイルスの作製とマウスの免疫化
呈递犬新孢子虫抗原蛋白的杆状病毒的制备及小鼠免疫
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [大月 隆寛, 董 金華, 加藤 竜也, 高坂 哲也, 朴 龍洙]
通讯作者: 朴 龍洙
BmNPVバクミド‐カイコ発現系を用いたNeospora caninum 抗原タンパク質の発現
BmNPV杆粒-家蚕表达系统表达犬新孢子虫抗原蛋白
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [S. Ito, H. E. Kato, S. Ohishi, R. Taniguchi, T. Iwata, O. Nureki, H. Kandori, 新井亮一, 大月 隆寛,加藤 竜也,朴 龍洙]
通讯作者: 大月 隆寛,加藤 竜也,朴 龍洙
32
    Development of tetravalent virus-like particle vaccine corresponding to four serotype dengue virus from silkworm
    • 批准号:
      16K14900
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.33万
    • 财政年份:
      2016
    • 负责人:
      PARK Enoch Y.
    • 依托单位:
    Basic research on vaccine development for protozoan infectious disease treatment using polyvalent virus-like particles with high immune response
    • 批准号:
      16H02544
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $25.63万
    • 财政年份:
      2016
    • 负责人:
      PARK Enoch Y.
    • 依托单位:
    Development of humanized sugar chain in silkworm targeting for production of next-generation medical glycoprotein
    • 批准号:
      23658286
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.41万
    • 财政年份:
      2011
    • 负责人:
      PARK Enoch Y.
    • 依托单位:
    海外基金