國家衛生研究院 NHRI:Item 3990099045/4662
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 12145/12927 (94%)
造访人次 : 907346      在线人数 : 908
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧：
  • 您可在西文检索词汇前后加上"双引号"，以获取较精准的检索结果
  • 若欲以作者姓名搜寻，建议至进阶搜寻限定作者字段，可获得较完整数据
    •  进阶搜寻
    主页 ‧ 登入 ‧ 上传 ‧ 说明 ‧ 关于NHRI ‧ 管理 到手机版


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/4662


    题名: Application of recombinant bamboo mosaic virus as vaccine to induce protective immunity in swine against foot-and-mouth disease virus
    作者: Yang, CD;Liao, JT;Jong, MH;Liang, CM;Lin, YL;Lin, NS;Hsu, YH;Liang, SM
    贡献者: Division of Molecular and Genomic Medicine
    摘要: Introduction: Plant viruses can be employed as versatile vectors for produc-tion of vaccines by expressing immunogenic epitopes on the surface of chi-meric viral particles. Although several viruses, including tobacco mosaicvirus, potato virus X and cowpea mosaic virus, have been developed as vectors, we aimed to develop a new viral vaccine delivery system, a bamboomosaic virus (BaMV), that carries larger transgene loads, and generates better immunity in the target animals with fewer adverse environmental effects.Methods: We engineered the BaMV as a vaccine vector expressing the anti-genic epitope(s) of the capsid protein VP1 of foot-and-mouth disease virus(FMDV). The recombinant BaMV plasmid (pBVP1) was constructed by replacing DNA encoding the 35 N-terminal amino acid residues of the BaMV coat protein with that encoding 37 amino acid residues (T128-N164)of FMDV VP1.Results: The pBVP1 infected host plants and generated a chimeric virionBVP1 expressing VP1 epitopes in its coat protein. Immunization of swine with BVP1 virions resulted in the production of anti-FMDV neutralizing antibodies and VP1-specific IFN-c. Furthermore, all BVP1-immunized swinewere protected against FMDV challenge. Conclusions: Chimeric BaMV virions that express partial sequence of FMDV VP1 effectively induced not only humoral and cell-mediated immune responses but also full protection against FMDV in target animals. This BaMV-based vector technology may be applied to other vaccines that require correct expression of antigens on chimeric viral particles.
    日期: 2008-06
    關聯: FEBS Journal. 2008 Jun;275(Suppl. 1 ):362.
    Link to: http://dx.doi.org/10.1111/j.1742-4658.2008.06448.x
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1742-464X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000256633301260
    显示于类别:[梁啟銘(2006-2007)] 會議論文/會議摘要

    文件中的档案:

    档案 描述 大小格式浏览次数
    ISI000256633301260.pdf62KbAdobe PDF672检视/开启


    在NHRI中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈