Regulating the immune response to tumours

被引:63
作者
Betts, Gareth J. [1 ]
Clarke, Sarah L. [1 ]
Richards, Hannah E. [1 ]
Godkin, Andrew J. [1 ]
Gallimore, Awen M. [1 ]
机构
[1] Univ Cardiff Wales, Dept Med Biochem & Immunol, Cardiff CF14 4XN, Wales
基金
英国医学研究理事会;
关键词
tumour immunity; T regulatory cells;
D O I
10.1016/j.addr.2006.05.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Naturally occurring regulatory T cells (Tregs) have been shown to suppress immune responses to self-antigens, thereby limiting autoimmunity. In the case of tumours, where immune responses to self-antigens are beneficial and lead to elimination of the tumour, such suppressive activity is actually detrimental to the host. Manipulation of Tregs holds great promise for the immunotherapy of cancer. Several studies performed using rodent models and indicate that Tregs cells inhibit effective antitumour immune responses and that their removal promotes tumour rejection. The increasing number of studies of Tregs in patients with cancer also point to a role for these cells in promoting disease progression. This review summarises the findings of these studies and addresses the advantages and potential pitfalls of manipulating Treg activity for the treatment of cancer. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:948 / 961
页数:14
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