Multi-epitope DNA vaccines

被引:71
作者
Suhrbier, A [1 ]
机构
[1] QUEENSLAND INST MED RES, COOPERAT RES CTR VACCINE TECHNOL, BRISBANE, QLD 4006, AUSTRALIA
关键词
cytotoxic T lymphocyte; DNA; EBV; epitope; HIV; melanoma; polytope; vaccine;
D O I
10.1038/icb.1997.63
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolution of vaccine strategies has seen a move from whole organisms to recombinant proteins, and further towards the ultimate in minimalist vaccinology, the epitope. The epitope-based approach is clearly compelling as only a relatively tiny, but immunologically relevant, sequence is often capable of inducing protective immunity against a large and complex pathogen. The post-reductionist era in epitope-based vaccinology has seen a quest to re-construct complexity and design vaccines containing many epitopes. The hope is that such multi-epitope vaccines might induce immunity against multiple antigenic targets, multiple strain variants, and/or even multiple pathogens. The ability of DNA vaccination to co-deliver a series of antibody and/or CD4 T cell epitopes remains largely unexplored, Successful viral vector and DNA-based experimental vaccines coding for multiple contiguous CD8 CTL epitopes have, however, recently been described. This simple CTL poly-epitope (or polytope) strategy may find application in the design of vaccines against several diseases including EBV, HIV and cancer.
引用
收藏
页码:402 / 408
页数:7
相关论文
共 103 条
[1]   Chemokines: Leucocyte recruitment and activation cytokines [J].
Adams, DH ;
Lloyd, AR .
LANCET, 1997, 349 (9050) :490-495
[2]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[3]   T-CELL PRIMING VERSUS T-CELL TOLERANCE INDUCED BY SYNTHETIC PEPTIDES [J].
AICHELE, P ;
BRDUSCHARIEM, K ;
ZINKERNAGEL, RM ;
HENGARTNER, H ;
PIRCHER, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (01) :261-266
[4]   Selective expansion of high- or low-avidity cytotoxic T lymphocytes and efficacy for adoptive immunotherapy [J].
AlexanderMiller, MA ;
Leggatt, GR ;
Berzofsky, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4102-4107
[5]   A multivalent minigene vaccine, containing B-cell, cytotoxic T-lymphocyte, and T-h epitopes from several microbes, induces appropriate responses in vivo and confers protection against more than one pathogen [J].
An, LL ;
Whitton, JL .
JOURNAL OF VIROLOGY, 1997, 71 (03) :2292-2302
[6]   Evolution and plasticity of CTL responses against HIV [J].
Autran, B ;
Hadida, F ;
Haas, G .
CURRENT OPINION IN IMMUNOLOGY, 1996, 8 (04) :546-553
[7]  
BARNES J, 1995, INPHARMA WEEKLY 0506, V985, P11
[8]   IN-VITRO PRIMING OF CYTOTOXIC T-LYMPHOCYTES AGAINST POORLY IMMUNOGENIC EPITOPES BY ENGINEERED ANTIGEN-PRESENTING CELLS [J].
BELLONE, M ;
IEZZI, G ;
MANFREDI, AA ;
PROTTI, MP ;
DELLABONA, P ;
CASORATI, G ;
RUGARLI, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (11) :2691-2698
[9]   SUBJUGATION OF DOMINANT IMMUNOGENIC DETERMINANTS WITHIN A CHIMERIC PEPTIDE [J].
BHARDWAJ, V ;
KUMAR, V ;
GEYSEN, HM ;
SERCARZ, EE .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (08) :2009-2016
[10]   Human tumor antigens recognized by T lymphocytes [J].
Boon, T ;
vanderBruggen, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :725-729