Cytokine-based transformation of immune surveillance into tumor-promoting inflammation

被引:0
|
作者
J B Mumm
M Oft
机构
[1] Schering-Plough Biopharma (formerly DNAX),Department of Oncology
来源
Oncogene | 2008年 / 27卷
关键词
IL-23; IL-12; Th17; inflammation; tumor immune surveillance;
D O I
暂无
中图分类号
学科分类号
摘要
During the last decade, it has become clear that the mammalian immune system is able to recognize and partially suppress nascent tumors. Human T cells specific to oncogenes and onco-fetal antigens are present in human cancer patients and their tumors. At the same time, molecular links between tumor-associated inflammation and tumor progression have been uncovered, providing an explanation for the long recognized epidemiological link between inflammation and cancer. The synopsis of these findings suggests a new interpretation of tumor immunity. It appears that antigen recognition or antigen-specific T-cell expansion at large is not as profoundly impaired in tumor patients as the correct polarization, the survival and the effector function of tumor-infiltrating T cells. This review will focus on pro-inflammatory cytokines likely to contribute to the deregulation of tumor-specific immunity and its consequences.
引用
收藏
页码:5913 / 5919
页数:6
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