Improved immunogenicity of DNA vaccination with mycobacterial HSP65 against bovine tuberculosis by protein boosting

被引:44
作者
Vordermeier, HM [1 ]
Lowrie, DB
Hewinson, RG
机构
[1] Vet Labs Agcy, TB Res Grp, Weybridge KT15 3NB, Surrey, England
[2] Natl Inst Med Res, London NW7 1AA, England
关键词
Mycobacterium tuberculosis; cattle-bacteria; vaccination; immunogenicity;
D O I
10.1016/S0378-1135(03)00046-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A scientific review for the government of the United Kingdom has recommended that the development of a cattle vaccine against bovine tuberculosis holds the best prospects to control this disease in the national herd. As BCG vaccination of cattle results in variable degrees of protection, novel vaccine strategies that could replace or supplement BCG are required. In this study, the mycobacterial antigen HSP65 was used to determine whether priming cattle with a plasmid DNA vaccine and subsequently boosting with the recombinant protein in adjuvant (heterologous prime-boost approach) would result in improved and more homogenous immune responses over immunising with plasmid DNA or protein in adjuvant alone. The results demonstrated that strong, and compared to protein or DNA vaccination protocols alone, more homogenous, cellular immune responses were induced in cattle vaccinated with the prime-boost regimen. In addition, DNA prime-protein boost vaccination as well as protein vaccination resulted in stronger humoral immune responses with a balanced IgG profile compared to DNA vaccination alone. Importantly, none of the vaccination protocols sensitised cattle to the intradermal tuberculin test suggesting that TB subunit vaccines can be designed to allow the continued use of the tuberculin test to discriminate between vaccinated cattle and those infected with Mycobacterium bovis. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:349 / 359
页数:11
相关论文
共 29 条
[1]  
Buddle BM, 1999, CLIN DIAGN LAB IMMUN, V6, P1
[2]   Vaccination of cattle against Mycobacterium bovis [J].
Buddle, BM .
TUBERCULOSIS, 2001, 81 (1-2) :125-132
[3]  
CLARKE GM, 1994, CONFIDENCE INTERVALS
[4]   Gene gun intradermal DNA immunization followed by boosting with modified vaccinia virus Ankara:: enhanced CD8+T cell immunogenicity and protective efficacy in the influenza and malaria models [J].
Dégano, P ;
Schneider, J ;
Hannan, CM ;
Gilbert, SC ;
Hill, AVS .
VACCINE, 1999, 18 (7-8) :623-632
[5]  
Doherty ML, 1996, IMMUNOLOGY, V87, P9
[7]   Priming by DNA immunization augments protective efficacy of Mycobacterium bovis bacille Calmette-Guerin against tuberculosis [J].
Feng, CG ;
Palendira, U ;
Demangel, C ;
Spratt, JM ;
Malin, AS ;
Britton, WJ .
INFECTION AND IMMUNITY, 2001, 69 (06) :4174-4176
[8]   Immunology of tuberculosis [J].
Flynn, JL ;
Chan, J .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :93-129
[9]  
Francis J., 1947, Bovine Tuberculosis including a contrast with Human Tuberculosis
[10]   Enhancement of MHC class I-restricted peptide-specific T cell induction by a DNA prime MVA boost vaccination regime [J].
Hanke, T ;
Blanchard, TJ ;
Schneider, J ;
Hannan, CM ;
Becker, M ;
Gilbert, SC ;
Hill, AVS ;
Smith, GL ;
McMichael, A .
VACCINE, 1998, 16 (05) :439-445