Th9 cells promote antitumor immune responses in vivo

被引:286
|
作者
Lu, Yong
Hong, Sungyoul
Li, Haiyan
Park, Jungsun
Hong, Bangxing
Wang, Lijuan
Zheng, Yuhuan
Liu, Zhiqiang
Xu, Jingda
He, Jin
Yang, Jing
Qian, Jianfei
Yi, Qing [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Div Canc Med, Houston, TX 77030 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2012年 / 122卷 / 11期
关键词
REGULATORY T-CELLS; DENDRITIC CELLS; ESTABLISHED MELANOMA; IL-9; PRODUCTION; TUMOR-IMMUNITY; HELPER-CELLS; TH17; CELLS; TGF-BETA; DISEASE; DIFFERENTIATION;
D O I
10.1172/JCI65459
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Th9 cells are a subset of CD4(+) Th cells that produce the pleiotropic cytokine IL-9. IL-9/Th9 can function as both positive and negative regulators of immune response, but the role of IL-9/Th9 in tumor immunity is unknown. We examined the role of IL-9/Th9 in a model of pulmonary melanoma in mice. Lack of IL-9 enhanced tumor growth, while tumor-specific Th9 cell treatment promoted stronger antitumor responses in both prophylactic and therapeutic models. Th9 cells also elicited strong host antitumor CD8(+) CTL responses by promoting Ccl20/Ccr6-dependent recruitment of DCs to the tumor tissues. Subsequent tumor antigen delivery to the draining LN resulted in CD8(+) T cell priming. In agreement with this model, Ccr6 deficiency abrogated the Th9 cell-mediated antitumor response. Our data suggest a distinct role for tumor-specific Th9 cells in provoking CD8(+) CTL-mediated antitumor immunity and indicate that Th9 cell-based cancer immunotherapy may be a promising therapeutic approach.
引用
收藏
页码:4160 / 4171
页数:12
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