Cytotoxic T cell polyepitope vaccines delivered by ISCOMs

被引:43
作者
Le, TTT
Drane, D
Malliaros, J
Cox, JC
Rothel, L
Pearse, M
Woodberry, T
Gardner, J
Suhrbier, A
机构
[1] Queensland Inst Med Res, Australian Natl Ctr Int & Trop Hlth & Nutr, Cooperat Res Ctr Vaccine Technol, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Brisbane, Qld 4029, Australia
[3] CSL Ltd, Div Res & Dev, Parkville, Vic 3052, Australia
基金
英国医学研究理事会;
关键词
ISCOM; polytope; cytotoxic T lymphocyte;
D O I
10.1016/S0264-410X(01)00243-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8 alpha beta cytotoxic T lymphocyte (CTL) polyepitope or polytope vaccines have traditionally been delivered using recombinant vector or DNA based delivery modalities. Here we show the delivery of polytope vaccines in the form of either synthetic polypeptides or recombinant polytope proteins by ImmunoStimulatory COMplexes (ISCOMs (R)). Induction of multiple protective CTL responses by these polytope-ISCOM formulations were comparable to viral vector or DNA based delivery modalities as assessed by IFN gamma ELISpot, chromium release and viral challenge assays. Measurement of CTL responses specific for the different epitopes revealed imunodominance patterns, which were largely independent of the vaccine vector or the order of the epitopes in the polytope. ISCOMs thus emerge as a viable human delivery modality for protein-based polytope vaccines. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4669 / 4675
页数:7
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