期刊文献+

口服丙型肝炎复合多表位DNA减毒鼠伤寒沙门活菌苗的实验研究 被引量:4

Immunogenicity of a multi epitopes antigen gene of hepatitis C virus carried by attenuated Salmonella typhimurium SL3261
原文传递
导出
摘要 目的 利用减毒鼠伤寒沙门菌作为载体,探讨丙型肝炎病毒(HCV) 口服DNA 疫苗的可行性。方法 把HCV 复合多表位抗原基因PCX 克隆到真核表达载体pcDNA3(CMV 启动子) ,构建HCV 真核表达载体pcDNA3/PCX,转化减毒鼠伤寒沙门菌SL3261 ,获得HCV 重组口服DNA 活菌苗SL3261 (pcDNA3/PCX) ,免疫小鼠及家兔后,检测特异性免疫应答及安全性。结果 SL3261(pcDNA3/PCX) 在小鼠及家兔中均可诱发低水平的特异性体液免疫及细胞免疫应答,免疫动物未见明显的毒性反应。结论 HCV 口服减毒鼠伤寒沙门菌DNA 疫苗可诱发特异性的免疫应答,为HCV Objective To use Salmonella typhimurium as a vehicle to explore the possibility of oral live DNA vaccine against hepatitis C virus (HCV).Methods A multi epitopes antigen gene of HCV was cloned into a eukaryotic vector pcDNA3 and introduced into attenuated Salmonella typhimurium SL3261 to construct HCV oral live DNA vaccine candidate SL3261 (pcDNA3/PCX). The recombinant bacterium was used to orally immunize mice and rabbits. Meanwhile, specific humoral and cellular immune responses and safety were detected.Results Low level of specific antibodies and cellular immune responses were induced without obvious toxicity in the immunized mice and rabbits after oral administration of the live bacteria.Conclusion The results indicate that the HCV recombinant oral live DNA vaccine can induce specific immune responses which might be able to provide an alternative for HCV vaccines.
出处 《中华传染病杂志》 CAS CSCD 北大核心 1999年第4期234-237,共4页 Chinese Journal of Infectious Diseases
基金 国家自然科学基金
关键词 丙型肝炎病毒 口服DNA疫苗 多表位疫苗 Hepatitis C virus Oral DNA vaccine Multi epitopes vaccine Immune response
  • 相关文献

参考文献5

二级参考文献3

共引文献8

同被引文献80

  • 1骆利敏,李明,夏虎,黄建生,陈百虹,王萍.乙型肝炎病毒多表位治疗性抗原基因的合成、表达及抗原性研究[J].第一军医大学学报,2003,23(8):802-805. 被引量:7
  • 2邓涛,范公忍,陈天宝,陈乃玲,胡大荣,王孟薇,贾克明.丙型肝炎病毒及乙型肝炎病毒联合基因免疫实验研究[J].中华医学杂志,2002,82(2):77-80. 被引量:9
  • 3Suhrbier A. Multi-epitope DNA vaccines[J]. Immunol Cell Biol, 1997,75(4) : 402. 被引量:1
  • 4An LL, Whitton JL. Multivalent minigene vaccines against infectious diseasel[J]. Curr Opin Mol Ther, 1999.1(1):16. 被引量:1
  • 5Smith SG. The polyepitope approach to DNA vaccination[J]. Curr Opin Mol Ther, 1999,1(1): 10. 被引量:1
  • 6Yu Z, Karem KL, Kanangat S. Protection by minigenes:a novel approach of DNA vaccines[J]. Vaccine,19980 16(17) :1660. 被引量:1
  • 7Sidney J, Grey HM, Kubo RT, et al. Practical, biochemical and evolutionary implications of the discovery of HLA class I supermotifs[J]. Immunol Today, 1996, 17(6) :261. 被引量:1
  • 8Fomsgaard A. Nielsen HV. Kirkby N, et al. Induction of cytotoxic T-cell responses by gene gun DNA vaccination with minigenes encoding influenza A virus HA and NP CTL-epitopes[J]. Vaccine,1999, 18(7-8) : 681. 被引量:1
  • 9Hanke T, Blanchard TJ, Schneider J, et al. Immunogenicities of intravenous and intramuscular administrations of MVA-based multi-CTL epitope vaccine for HIV in mice[J]. J Gen Virol,1998, 79(Ptl): 83. 被引量:1
  • 10Hanke T, McMichael A. Pre-clinical development of a multi-CTL epitope-based DNA prime MVA boost vaccine for AIDS[J]. Immunol Lett,1999, 66(1-3): 177. 被引量:1

引证文献4

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部