Tumour immunology, vaccination and escape strategies

被引:43
作者
García-Lora, A
Algarra, I
Collado, A
Garrido, F
机构
[1] Univ Granada, Hosp Univ Virgen Nieves, Serv Anal Clin, E-18014 Granada, Spain
[2] Univ Jaen, Dept Ciencias Salud, Jaen, Spain
[3] Univ Granada, Hosp Univ Virgen Nieves, Unidad Invest, E-18014 Granada, Spain
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 2003年 / 30卷 / 03期
关键词
D O I
10.1046/j.1365-2370.2003.00384.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Our increasing knowledge of the mechanisms by which tumour cells escape immune effector cells is helping to establish new approaches to therapeutic vaccination against tumour development. One of the escape mechanisms used by tumour cells is the generation of multiple variants with different HLA phenotypes. These MHC class I phenotypic alterations play a key role in the tumour-host scenario, as they are crucial molecules for antigen presentation to T cells and modulation of natural killer (NK) cell activity. This review presents evidence indicating that tumours develop sophisticated MHC phenotypes that allow them to escape immune surveillance. We evaluate the importance of these alterations in terms of the potential development of therapeutic approaches to immune vaccination.
引用
收藏
页码:177 / 183
页数:7
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