Optimal conditions required for influenza A infection-enhanced cross-priming of CD8+ T cells specific to cell-associated antigens

被引:2
|
作者
Wei, Joe [1 ]
Waithman, Jason [2 ]
Xiao, Kun [3 ]
Oveissi, Sara [3 ]
Chen, Weisan [3 ]
机构
[1] Austin Hlth, Melbourne Austin Branch, Ludwig Inst Canc Res, Melbourne, Vic, Australia
[2] Univ Western Australia, Ctr Child Hlth Res, Telethon Inst Child Hlth Res, Perth, WA 6009, Australia
[3] La Trobe Univ, Sch Mol Sci, Cell Lab T, Melbourne, Vic 3086, Australia
来源
IMMUNOLOGY AND CELL BIOLOGY | 2013年 / 91卷 / 09期
基金
澳大利亚国家健康与医学研究理事会;
关键词
cross-priming; influenza A virus; melanoma; tumour; DENDRITIC CELLS; CLASS-I; EXOGENOUS ANTIGENS; RESPONSES; CANCER; TOLERANCE; IMMUNOTHERAPY; INTERFERON; PROTEINS; IMMUNITY;
D O I
10.1038/icb.2013.46
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dendritic cells can take up exogenous tumor antigens and present their antigenic epitopes to CD8(+) T cells (TCD8(+)), a process called cross-presentation. Cross-presentation is especially important in antitumor immunity because tumor cells, although carrying tumor antigens, do not activate naive T cells efficiently because of a lack of co-stimulatory molecules. Our group has recently shown that influenza A virus (IAV) infection of allogeneic cells lead to enhanced cross-priming of TCD8(+) specific to cellular antigens. To develop this into a potential vaccine strategy, in this study, we have systematically investigated the numbers of allogeneic cells infected by IAV, IAV doses and their infectious activity, the length of in vitro infection and other associated factors. We have defined the optimal immune-enhancing conditions and we have also shown in vivo that such enhanced cross-priming did lead to enhanced tumor protection. The knowledge should be useful for developing more robust cancer vaccine.
引用
收藏
页码:576 / 582
页数:7
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