The Multifaceted Role of Th17 Lymphocytes and Their Associated Cytokines in Cancer

被引:36
作者
Alizadeh, Darya [1 ,2 ]
Katsanis, Emmanuel [1 ,2 ,3 ,4 ]
Larmonier, Nicolas [1 ,2 ,3 ,4 ]
机构
[1] Univ Arizona, Canc Biol Grad Interdisciplinary Program, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Pediat, Steele Childrens Res Ctr, Tucson, AZ 85724 USA
[3] Univ Arizona, Dept Immunobiol, Inst BIO5, Tucson, AZ 85724 USA
[4] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2013年
关键词
REGULATORY T-CELLS; GROWTH-FACTOR-BETA; TGF-BETA; T(H)17 CELLS; IFN-GAMMA; HEPATOCELLULAR-CARCINOMA; TRANSCRIPTION FACTOR; TUMOR-GROWTH; GM-CSF; DEVELOPMENTAL PLASTICITY;
D O I
10.1155/2013/957878
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
While the role of T helper 17 lymphocytes (Th17) in the pathogenesis of autoimmune diseases and in infectious immunity has been relatively well defined, the impact of these cells and their associated cytokines on cancer development is still under debate. Although multiple reports have indicated that Th17 can promote anticancer immunity, others have argued that these cells may exhibit tumor-promoting properties. This dichotomy in the function of Th17 lymphocytes in cancer may be related to the versatile nature of these cells, being capable of differentiating into either proinflammatory Th1 or suppressive FoxP3-expressing Treg cells or hybrid T cell subsets depending on the underlying environmental conditions. In the current review, we examine the role of Th17 lymphocytes and Th17-associated cytokines in cancer and discuss how factors that control their final lineage commitment decision may influence the balance between their tumor-promoting versus tumor-suppressing properties.
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页数:11
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