Effect of pre-existing cytotoxic T lymphocytes on therapeutic vaccines

被引:0
|
作者
Sherritt, MA
Gardner, J
Elliott, SL
Schmidt, C
Purdie, D
Deliyannis, G
Heath, WR
Suhrbier, A
机构
[1] Australian Natl Ctr Int Trop Hlth & Nutr, Cooperat Res Ctr Vaccine Technol, Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Royal Brisbane Hosp, Brisbane, Qld 4029, Australia
[3] Queensland Inst Med Res, Epidemiol & Populat Hlth Unit, Brisbane, Qld 4006, Australia
[4] Univ Melbourne, Dept Microbiol & Immunol, VT, CRC, Parkville, Vic 3052, Australia
[5] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Div Immunol, VT,CRC, Parkville, Vic 3050, Australia
关键词
cytotoxic T lymphocyte; therapeutic vaccine; immunodominance; polytope;
D O I
10.1002/1521-4141(200002)30:2<671::AID-IMMU671>3.0.CO;2-H
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Therapeutic vaccines which aim to induce CD8(+) cytotoxic T lymphocyte (CTL) responses will often be required to perform in the presence of pre-existing CTL which recognize epitopes within the vaccine. Here we explore the ability of a viral vaccine vector presenting several co-dominant CTL epitopes to prime CTL responses in animals that have a pre-existing CTL response to one of the epitopes in the vaccine. The vaccine was usually capable of inducing multiple new responses, suggesting that immunodomination effects of pre-existing CTL may generally be minimal following vaccination. However, when large numbers of pre-existing CTL were present, a novel type of immune modulation was observed whereby (1) the vaccine failed to prime efficiently new CTL responses that were restricted by the same MHC gene as the pre-existing responses, and (2) vaccine-induced CTL responses restricted by other MHC genes were enhanced. These results may have implications for therapeutic multi-epitope vaccines for diseases like HIV and melanoma, which aim to broaden CTL responses.
引用
收藏
页码:671 / 677
页数:7
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