Intratumoral immunotherapy: using the tumour against itself

被引:59
作者
Crittenden, MR
Thanarajasingam, U
Vile, RG
Gough, MJ
机构
[1] Mayo Clin, Program Mol Med, Rochester, MN USA
[2] Mayo Clin, Dept Immunol, Rochester, MN USA
关键词
chemokine; dendritic cell; immunotherapy; T cell; tumour;
D O I
10.1111/j.1365-2567.2004.02001.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Diverse immunotherapy approaches have achieved success in controlling individual aspects of immune responses in animal models. Transfer of such immunotherapies to clinical trials has obtained some success in patients, with clinical responses observed or effective antigen specific immune responses achieved, but has had limited impact on patient survival. Key elements required to generate de novo cell-mediated antitumour immune responses in vivo include recruitment of antigen-presenting cells to the tumour site, loading these cells with antigen, and their migration and maturation to full antigen-presenting function. In addition, it is essential for antigen-specific T cells to locate the tumour to mediate cytotoxicity, emphasizing the need for local inflammation to target effector cell recruitment. We review those therapies that involve the tumour site as a target and source of antigen for the initiation of immune responses, and discuss strategies to generate and co-ordinate an optimal cell-mediated immune response to control tumours locally.
引用
收藏
页码:11 / 22
页数:12
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