CD25+ regulatory T cells and tumor immunity

被引:23
作者
Jones, E
Dahm-Vicker, M
Golgher, D
Gallimore, A
机构
[1] John Radcliffe Hosp, Nuffield Dept Med, Oxford OX3 9DU, England
[2] Univ Southampton, Sch Med, Canc Sci Div, Southampton, Hants, England
基金
英国惠康基金;
关键词
immunogenicity; melanoma; mutations; tumor;
D O I
10.1016/S0165-2478(02)00240-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor cells express a range of antigens including self-antigens (those whose expression is shared by normal host tissue) and non-self antigens (such as those that arise as a result of mutations in normal cellular genes or in the case of some tumors, viral antigens). Immune responses to both types of antigen have been identified in human patients with cancer and in murine tumor models. In both cases, these responses are typically weak and generally fail to result in tumor rejection. Accumulating evidence indicates that a population of T cells, namely CD25(+) regulatory cells, is at least Partly responsible for the poor immunogenicity of tumor cells. This evidence is discussed in the context of a marine model of melanoma. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:141 / 143
页数:3
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