Regulatory T Cells: Major Players in the Tumor Microenvironment

被引:65
作者
Beyer, Marc [1 ]
Schultze, Joachim L. [1 ]
机构
[1] Univ Bonn, Lab Genom & Immunoregulat, LIMES Inst, D-53115 Bonn, Germany
关键词
Regulatory T cells; tumor immunology; FOXP3; HIGH-DOSE INTERLEUKIN-2; PLASMACYTOID DENDRITIC CELLS; COLONY-STIMULATING FACTOR; TGF-BETA; INDOLEAMINE 2,3-DIOXYGENASE; CANCER-PATIENTS; IN-VIVO; MEDIATED SUPPRESSION; PERIPHERAL-BLOOD; IMMUNE-RESPONSES;
D O I
10.2174/138161209788453211
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the last years a number of reports have described elevated numbers of regulatory T (T-reg) cells inside of tumors, in close proximity of the tumor, draining lymph nodes and also in peripheral blood of patients with solid tumors and hematologic malignancies. There is increasing evidence that T-reg cells can migrate into tumors and suppress effective anti-tumor responses in the tumor microenvironment, thus contributing to the prosperity and growth of human tumors. In addition, several mechanisms have been described how conversion of conventional CD4(+) T cells into T-reg cells can occur in the context of human tumors, yet little is known about the molecular and cellular features responsible for the increase and maintenance of elevated levels of T-reg cells in cancer. Recent studies now have elucidated how T-reg cells mediate regulatory activity in the tumor microenvironment and enhanced our understanding of the underlying molecular mechanisms. Targeting T-reg cells therefore provides an attractive therapeutic strategy to potentially influence the suppressed immune response in tumor patients thereby altering and supporting anti-tumor therapy.
引用
收藏
页码:1879 / 1892
页数:14
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