期刊文献+

新型腺病毒载体肺结核疫苗的免疫原性研究 被引量:3

Immunogenicity study of novel Ad5 based tuberculosis vaccine
下载PDF
导出
摘要 目的:评价双价肺结核疫苗的免疫原性。方法:ESAT6、rv3407、RpfB三种抗原基因融合后(TPA-3Ag)与Ag85A一种抗原基因均用重组人5型腺病毒载体进行表达,按照1∶0.2、1∶1、1∶2、1∶4四种不同滴度配比免疫小鼠。使用酶联免疫吸附实验(ELISA)进行抗原特异性体液免疫评价,使用酶联免疫斑点法(ELISpot)和细胞内细胞因子染色(ICS)进行抗原特异性细胞免疫评价。结果:双价疫苗均产生体液免疫应答和细胞免疫应答。结论:双价疫苗有提高肺结核保护范围的可能性,可能成为预防结核病的新型疫苗。 Objective:To evaluate the immunogenicity of bivalent tuberculosis vaccine.Methods:ESAT6,rv3407 and RpfB three antigen gene fusion(TPA-3Ag)and Ag85A an antigen gene were expressed by recombinant human type 5 adenovirus vector,according to 1∶0.2,1∶1,1∶2 and 1∶4 four different titer ratios to immunize mice.Antigen-specific humoral immunoassay using enzyme-linked immunosorbent assay(ELISA),antigen-specific cellular immune evaluation using enzyme-linked immunospot assay(ELISpot)and intracellular cytokine staining(ICS).Results:Bivalent vaccines produce both humoral and cellular immune responses.Conclusion:Bivalent vaccine have the potential to increase the scope of tuberculosis protection and may become a new vaccine against tuberculosis.
作者 史晓雨 隋秀文 苗伟 高德进 王畅 魏梦函 朱涛(指导) SHI Xiao-Yu;SUI Xiu-Wen;MIAO Wei;GAO De-Jin;WANG Chang;WEI Meng-Han;ZHU Tao(Tianjin University of Science & Technology,Tianjin 300457,China)
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2020年第6期719-722,共4页 Chinese Journal of Immunology
基金 国家科技重大专项项目(2018ZX10731301-001-002)。
关键词 人5型腺病毒 ESAT6 rv3407 RpfB AG85A 肺结核 Human adenovirus 5 ESAT6 rv3407 RpfB Ag85A Tuberculosis
  • 相关文献

参考文献2

二级参考文献37

  • 1World Health Organization. Tuberculosis[M].Geneva:World Health Organization,2008.
  • 2World Health Organization. Global Tuberculosis Control:Epidemiology,Strategy,Financing[M].Geneva:World Health Organization,2009.
  • 3Behr MA,Wilson MA,Gill WP. Comparative genomics of BCG vaccines by whole-genome DNA microarray[J].Science,1999,(5419):1520-1523.
  • 4Svenson S,K(a)llenius G,Pawlowski A. Towards new tuberculosis vaccines[J].Hum Vaccin,2010,(04):309-317.
  • 5Brewer TF. Preventing tuberculosis with bacillus Calmette-Guérin vaccine:a meta-analysis of the literature[J].Clinical Infectious Diseases,2000,(Suppl 3):S64-S67.
  • 6World Health Organization. Stop TB Partnership.The Global Plan to Stop TB[M].Geneva:World Health Organization,2009.
  • 7McShane H,Brookes R,Gilbert SC. Enhanced immunogenicity of CD4 (+) t-cell responses and protective efficacy of a DNA-modified vaccinia virus Ankara prime-boost vaccination regimen for murine tuberculosis[J].Infection and Immunity,2001,(02):681-686.
  • 8Havenga M,Vogels R,Zuijdgeest D. Novel replication-incompetent adenoviral B-group vectors:high vector stability and yield in PER.C6 cells[J].Journal of General Virology,2006,(Pt 8):2135-2143.
  • 9Wang J,Thorson L,Stokes RW. Single mucosal,but not parenteral,immunization with recombinant adenoviral-based vaccine provides potent protection from pulmonary tuberculosis[J].Journal of Immunology,2004,(10):6357-6365.
  • 10Wiker HG,Harboe M. The antigen 85 complex:a major secretion product of Mycobacterium tuberculosis[J].Microbiological Reviews,1992,(04):648-661.

共引文献1

同被引文献23

引证文献3

二级引证文献13

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