Vaccination of guinea pigs with DNA encoding Ag85A by gene gun bombardment

被引:21
作者
Sugawara, I
Yamada, H
Udagawa, T
Huygen, K
机构
[1] Res Inst TB, Dept Mol Pathol, Tokyo, Japan
[2] Inst Pasteur, B-1180 Brussels, Belgium
关键词
guinea pig; tuberculosis DNA vaccine; Ag85A; peptide boosting; aerosol infection;
D O I
10.1016/S1472-9792(03)00054-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A DNA vaccine encoding Ag85A from Mycobacterium tuberculosis was administered to guinea pigs by epidermal gene gun bombardment and its protective efficacy was determined. Vaccination with Ag85A DNA twice significantly reduced the severity of pulmonary pathology and number of pulmonary colony-forming units (CFU) (p<0.01). When immunogenic synthetic Ag85A peptide was used as a booster, lung pathology was improved significantly and pulmonary CFU were reduced dramatically. Neither Ag85A DNA nor BCG Tokyo protected the guinea pigs from hematogenous spread of tubercle bacilli to the spleen because splenic granulomas without central necrosis were recognized. When the vaccinated guinea pigs were followed up for 7 months, the pulmonary lesions became fibrotic in guinea pigs vaccinated with Ag85A DNA plus Ag85A peptide, or BCG Tokyo, and no tubercle bacilli were detected. The protective efficacy of the tuberculosis Ag85A DNA vaccine was improved significantly by peptide boosting. It is concluded that dosage and peptide boosting are important in the induction of higher protective efficacy by a tuberculosis DNA vaccine. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:331 / 337
页数:7
相关论文
共 20 条
  • [1] Evaluation of new vaccines in the mouse and guinea pig model of tuberculosis
    Baldwin, SL
    D'Souza, C
    Roberts, AD
    Kelly, BP
    Frank, AA
    Lui, MA
    Ulmer, JB
    Huygen, K
    McMurray, DM
    Orme, IM
    [J]. INFECTION AND IMMUNITY, 1998, 66 (06) : 2951 - 2959
  • [2] Bloom Barry R., 1994, P531
  • [3] Vaccination of guinea pigs with DNA encoding the mycobacterial antigen MPB83 influences pulmonary pathology but not hematogenous spread following aerogenic infection Mycobacterium bovis
    Chambers, MA
    Williams, A
    Hatch, G
    Gavier-Widén, D
    Hall, G
    Huygen, K
    Lowrie, D
    Marsh, PD
    Hewinson, RG
    [J]. INFECTION AND IMMUNITY, 2002, 70 (04) : 2159 - 2165
  • [4] HOST-PARASITE RELATIONSHIPS IN EXPERIMENTAL AIRBORNE TUBERCULOSIS .5. LACK OF HEMATOGENOUS DISSEMINATION OF MYCOBACTERIUM-TUBERCULOSIS TO LUNGS IN ANIMALS VACCINATED WITH BACILLUS CALMETTE-GUERIN
    FOK, JS
    HO, RS
    ARORA, PK
    HARDING, GE
    SMITH, DW
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1976, 133 (02) : 137 - 144
  • [5] Immunogenicity and protective efficacy of a tuberculosis DNA vaccine
    Huygen, K
    Content, J
    Denis, O
    Montgomery, DL
    Yawman, AM
    Deck, RR
    DeWitt, CM
    Orme, IM
    Baldwin, S
    DSouza, C
    Drowart, A
    Lozes, E
    Vandenbussche, P
    VanVooren, JP
    Liu, MA
    Ulmer, JB
    [J]. NATURE MEDICINE, 1996, 2 (08) : 893 - 898
  • [6] Kamath AT, 1999, INFECT IMMUN, V67, P1702
  • [7] Is the development of a new tuberculosis vaccine possible?
    Kaufmann, SHE
    [J]. NATURE MEDICINE, 2000, 6 (09) : 955 - 960
  • [8] BCG-INDUCED PROTECTION IN GUINEA-PIGS VACCINATED AND CHALLENGED VIA THE RESPIRATORY ROUTE
    LAGRANDERIE, M
    RAVISSE, P
    MARCHAL, G
    GHEORGHIU, M
    BALASUBRAMANIAN, V
    WEIGESHAUS, EH
    SMITH, DW
    [J]. TUBERCLE AND LUNG DISEASE, 1993, 74 (01): : 38 - 46
  • [9] Protection against tuberculosis by a plasmid DNA vaccine
    Lowrie, DB
    Silva, CL
    Colston, MJ
    Ragno, S
    Tascon, RE
    [J]. VACCINE, 1997, 15 (08) : 834 - 838
  • [10] The immunogenicity of single and combination DNA vaccines against tuberculosis
    Morris, S
    Kelley, C
    Howard, A
    Li, ZM
    Collins, F
    [J]. VACCINE, 2000, 18 (20) : 2155 - 2163