Ovalbumin lipid core peptide vaccines and their CD4+ and CD8+ T cell responses

被引:15
|
作者
Simerska, Pavia [1 ]
Suksamran, Tittaya [1 ]
Ziora, Zyta Maria [1 ]
Rivera, Fabian de Labastida [2 ]
Engwerda, Christian [2 ]
Toth, Istvan [1 ,3 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
[2] Queensland Inst Med Res, Immunol & Infect Lab, Herston, Qld 4029, Australia
[3] Univ Queensland, Sch Pharm, Pharm Australia Ctr Excellence, Woolloongabba, Qld 4102, Australia
基金
澳大利亚研究理事会;
关键词
Ovalbumin; Peptide synthesis; Vaccine development; CD4(+); CD8(+); T cell; IN-VIVO; ANTIGEN; INFECTION; CANCER; STIMULATION; ACTIVATION; TCR;
D O I
10.1016/j.vaccine.2014.06.049
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The lipid core peptide (LCP) system has successfully been used in development of peptide-based vaccines against cancer and infectious diseases (such as group A streptococcal infection). CD8(+) T cells are important targets for vaccines, however developing a vaccine that activates long-lasting immunity has proven challenging. The ability of LCP vaccines to activate antigen-specific CD8(+) and/or CD4(+) T cell responses was tested using compounds that contained two or four copies of OVA(257-264) and/or OVA(323-339) peptides conjugated to LCP, which are recognised by OTI (CD8(+) specific) and OTII (CD4(+) specific) T cells, respectively. The LCP ovalbumin vaccines developed in this study were synthesised in 30% yields and showed no significant haemolytic effect on red blood cells (below 4% haemolysis when tested with compounds at up to 100 mu M concentrations). Promising in vivo data in mice suggested that this LCP-ovalbumin vaccine system could act as a novel and potent vehicle for the stimulation of robust antigen-specific CD8(+) T cell responses. (C) 2014 Elsevier Ltd. All rights reserved.
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页码:4743 / 4750
页数:8
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