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结核分枝杆菌四价DNA疫苗免疫原性和保护效率研究 被引量:6

Study on Immunogenicity and Protective Efficacy of Tetravalent Combination M.tuberculosis DNA Vaccinea
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摘要 对结核杆菌四价DNA疫苗的免疫应答和保护效果进行了评价.用编码结核分枝杆菌Ag85B、MPT64、MPT70和PstS-3等4种抗原蛋白的基因分别构建的单价DNA疫苗混合成四价苗免疫小鼠.3次免疫后21天,四种抗原特异性抗体滴度分别达到1:6 400、1:51 200、1:6 400、1:6 400.四种蛋白质均能诱导脾脏细胞产生较高水平的抗原特异性IFN-γ,浓度分别为10 582.14 ng/L、13 635.97 ng/L、14 213.15 ng/L和9 657.35 ng/L.三次免疫后经静脉强毒攻击,四价苗组小鼠肺脏和脾脏的载菌数分别减少到阴性组的1/650和1/130.对肺组织的病理形态特征观察表明,空载体免疫的小鼠肺部严重损伤,肺实质干酪样坏死,坏死结节占肺实质的70%~80%,而四价苗免疫的小鼠,肺组织结构正常,肺泡轮廓清晰.研究首次证实,Ag85B、MPT64、MPT70和PstS-3 4种结核杆菌抗原蛋白编码基因组成的四价DNA疫苗,具有很高的免疫应答水平和保护效率. In order to evaluate the immunogenicity and protective efficacy of tetravalent combination M.tuberculosis DNA vaccine, DNA vaccines encoding Ag85B, MPT64, MPT70 and PstS-3 protein were constructed with eukaryotic expression vector pJW4303. Combination DNA vaccines were inoculated intramuscularly into C57BL/6 mice three times at 3 weeks interval. After 21 days of the third injection, the specific antibody titers against the four antigens were 1:6 400, 1:51 200, 1:6 400 and 1:6 400. Meanwhile the mixed spleen cells could produce the high antigen-specific IFN-gamma level in response to the four antigen proteins, IFN-gamma level of Ag85B, MPT64, MPT70 and PstS-3 reached 10 582.14 ng/L, 13 635.97 ng/L, 14 213.15 ng/L and 9 657.35 ng/L respectively. After the last injection, mice were challenged with M.tuberculosis H37Rv. When compared to negative group, the bacterial counts of lung and spleen from the mice vaccinated with tetravalent combination vaccine were reduced about 650 and 130 folds. Microphotographs showed clearly that lungs of mice vaccinated with combination vaccine were much better protected against Mycobacterium tuberculosis challenge than negative mice. The results showed that tetravalent combination M.tuberculosis DNA vaccine elicited both T-cell and humoral immune response, and protected against tuberculosis effectively.
出处 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2005年第4期347-352,共6页 Progress In Biochemistry and Biophysics
基金 国家高技术"863"计划资助项目(2002AA206411).~~
关键词 结核分枝杆菌 抗原蛋白 四价DNA疫苗 免疫原性 保护效率 PLASMID DNA VACCINATION PROTEIN GENE ANTIGEN-85 EPITOPE CLONING H37RV MPT64 BOVIS
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参考文献20

  • 1蔡宏,潘怡,朱玉贤,李国利,庄玉辉.结核分枝杆菌多价核酸疫苗的构建及免疫原性[J].科学通报,2002,47(13):966-971. 被引量:12
  • 2Wiker H G, Harboe M. The antigen 85 complex: a major secretion product of Mycobacterium TuBerculosis. Microbiological Reviews,1992, 56 (4): 648~661.
  • 3Tobias F, Wit R D, Bekelie S, et al. The Mycobacterium leprae antigen 85 complex gene family: identification of the genes for the 85A, 85C, and related MPT51 proteins. Infect Immun, 1993, 61 (9):3642~3647.
  • 4Roche P W, Peake P W, Jacobe H B, et al. T-Cell determinants and antibody binding sites on the major Mycobacterial secretory protein MPB59 of Mycobacterium bovis. Infect Immun, 1994, 62(12) :5319~5326.
  • 5Harth G, Lee B Y, Wang J, et al. Novel insight into the genetics,biochemistry, and immunocytochemistry of the 30-kilodalton major extracellular protein of Mycobacterium tuberculosis. Infect Immun,1996, 64 (8): 3038~3047.
  • 6Ulmer J B, Liu M A, Montgomery D L, et al. Expression and immunogenicity of Mycobacterium tuberculosis antigen 85 by DNA vaccination. Vaccine, 1997, 15 (8): 792~794.
  • 7Denis O, Tanghe A, Palfliet K, et al. Vaccination with plasmid DNA encoding Mycobacterial antigen 85A stimulates a CD4+ and CD8+T-cell epitopic repertoire broader than that stimulated by Mycobacterium tuberculosis H37Rv infection. Infect Immun, 1998,66 (7): 1527~1533.
  • 8Yamaguchi R, Matsuo K, Yamazaki A, et al. Cloning characterization of the gene for immunogenic protein MPB64 of Mycobacterium bovis BCG. Infect Immun, 1989, 57 (9): 283~288.
  • 9Oettinge T, Andersen A B. Cloning and B-cell-epitope mapping of MPT64 from Mycobacterium tuberculosis H37Rv. Infect Immun,1994, 62 (5): 2058~2064.
  • 10Oettinger T, Holm A, Mtoni I M, et al. Mapping of the delayed-type hypersensitivity-inducing epitope of secreted protein MPT64 from Mycobacterium tuberculosis. Infect Immun, 1995, 63 (12):4613~4618.

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