Short peptide sequences containing MHC class I and/or class II epitopes linked to nano-beads induce strong immunity and inhibition of growth of antigen-specific tumour challenge in mice

被引:64
作者
Fifis, T [1 ]
Mottram, P [1 ]
Bogdanoska, V [1 ]
Hanley, J [1 ]
Plebanski, M [1 ]
机构
[1] Austin Hosp, Austin Res Inst, Vaccine Dev & Infect Dis Unit, Heidelberg, Vic 3084, Australia
基金
英国医学研究理事会;
关键词
peptides; tumours; vaccine;
D O I
10.1016/j.vaccine.2004.05.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peptide based vaccines offer practical advantages, but unmodified peptides usually require an adjuvant or delivery vehicle to promote immunogenicity. When peptides containing ovalbumin (OVA) derived CD4 and CD8 T cell epitopes were conjugated to 0.05 mum nano-beads, they gave strong immune responses and inhibition of growth of tumour cells expressing the CD8 T cell epitope with MHC class I. These responses were inducible with both high (50 mug) and low (5 mug) peptide doses after a single immunisation. The helper CD4 T cell epitope was unnecessary for induction of CD8 T cell or tumour challenge responses. However, the CD4 T cell epitope contained a B cell epitope and triggered strong antibody responses. This simple approach offers a convenient experimental tool and a potentially useful clinical method for peptide immunisation. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:258 / 266
页数:9
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