Protection against Leishmania donovani infection by DNA vaccination:: increased DNA vaccination efficiency through inhibiting the cellular p53 response

被引:48
作者
Ghosh, A [1 ]
Labrecque, S [1 ]
Matlashewski, G [1 ]
机构
[1] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
p53; DNA vaccine; HPV E6; Leishmania;
D O I
10.1016/S0264-410X(01)00023-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA-vaccination holds great promise for the future of vaccine development against infectious diseases. especially in developing countries, We therefore investigated the possibility of using DNA-vaccination against Leishmania donovani infection with the A2 virulence gene and whether inhibiting the cellular p53 response could increase the effectiveness of the A2 DNA vaccine. p53, also known as the guardian of the genome, is activated following DNA transfection and has pleotropic effects on cells. which could have adverse effects on the effectiveness of DNA-vaccination. Two major observations are reported within. First, vaccination with the A2 gene induced both humoral and cellular immune responses against A2 which provided significant protection against infection with L. donovani. Second, inhibition of p53 with human papillomavirus E6 resulted in higher expression of heterologous transfected genes in vitro and more efficient DNA-vaccination in vivo. These results have important implications for DNA vaccination against leishmaniasis and potentially against other infectious diseases. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3169 / 3178
页数:10
相关论文
共 45 条
[1]   Regulation of p53 stability [J].
Ashcroft, M ;
Vousden, KH .
ONCOGENE, 1999, 18 (53) :7637-7643
[2]   VISCERAL LEISHMANIASIS - MORE PREVALENT AND MORE PROBLEMATIC [J].
BAILY, GG ;
NANDY, A .
JOURNAL OF INFECTION, 1994, 29 (03) :241-247
[3]  
Ballas ZK, 1996, J IMMUNOL, V157, P1840
[4]   ISOLATION OF HUMAN-P53-SPECIFIC MONOCLONAL-ANTIBODIES AND THEIR USE IN THE STUDIES OF HUMAN P53 EXPRESSION [J].
BANKS, L ;
MATLASHEWSKI, G ;
CRAWFORD, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (03) :529-534
[5]   Co-stimulation in T cell responses [J].
Chambers, CA ;
Allison, JP .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (03) :396-404
[6]   The developmental expression of Leishmania donovani A2 amastigote-specific genes is post-transcriptionally mediated and involves elements located in the 3'-untranslated region [J].
Charest, H ;
Zhang, WW ;
Matlashewski, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) :17081-17090
[7]   DEVELOPMENTAL GENE-EXPRESSION IN LEISHMANIA-DONOVANI - DIFFERENTIAL CLONING AND ANALYSIS OF AN AMASTIGOTE-STAGE-SPECIFIC GENE [J].
CHAREST, H ;
MATLASHEWSKI, G .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :2975-2984
[8]   Improvement of hepatitis B virus DNA vaccines by plasmids coexpressing hepatitis B surface antigen and interleukin-2 [J].
Chow, YH ;
Huang, WL ;
Chi, WK ;
Chu, YD ;
Tao, MH .
JOURNAL OF VIROLOGY, 1997, 71 (01) :169-178
[9]   Influence of Quillaja saponaria triterpenoid content on the immunomodulatory capacity of Epstein-Barr virus iscoms [J].
Dotsika, E ;
Karagouni, E ;
Sundquist, B ;
Morein, B ;
Morgan, A ;
VillacresEriksson, M .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1997, 45 (03) :261-268
[10]   Antibody response against a Leishmania donovani amastigote-stage-specific protein in patients with visceral leishmaniasis [J].
Ghedin, E ;
Zhang, WW ;
Charest, H ;
Sundar, S ;
Kenney, RT ;
Matlashewski, G .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1997, 4 (05) :530-535