CTLA4 blockade reduces immature myeloid cells in head and neck squamous cell carcinoma

被引:62
|
作者
Yu, Guang-Tao [1 ,2 ]
Bu, Lin-Lin [1 ,2 ]
Zhao, Yu-Yue [1 ,2 ]
Mao, Liang [1 ,2 ]
Deng, Wei-Wei [1 ,2 ]
Wu, Tian-Fu [3 ]
Zhang, Wen-Feng [3 ]
Sun, Zhi-Jun [1 ,2 ,3 ]
机构
[1] Minist Educ, State Key Lab Breeding Base Basic Sci Stomatol, Wuhan, Peoples R China
[2] Minist Educ, Key Lab Oral Biomed, Wuhan, Peoples R China
[3] Wuhan Univ, Sch & Hosp Stomatol, Dept Oral Maxillofacial Head Neck Oncol, Wuhan, Peoples R China
来源
ONCOIMMUNOLOGY | 2016年 / 5卷 / 06期
基金
中国国家自然科学基金;
关键词
CTLA4; HNSCC; immunotherapy; MDSCs; myeloid cells; M2; macrophages; REGULATORY T-CELLS; SUPPRESSOR-CELLS; NEGATIVE REGULATOR; CANCER; EXPRESSION; PD-1; MACROPHAGES; INHIBITION; MECHANISMS; CORRELATE;
D O I
10.1080/2162402X.2016.1151594
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immature myeloid cells such as myeloid-derived suppressor cells (MDSCs) and M2 macrophages play a vital role in the tumor immune escape and tumor progression. Cytotoxic T lymphocyte-associated antigen 4 (CTLA4), as a negative immune checkpoint, is highly expressed in numerous solid tumors. However, precise functions of CTLA4 in head and neck squamous cell carcinoma (HNSCC) have not yet been elucidated. In this study, we demonstrated that the ratio of CD8(+)/CTLA4 can be used as a potential index with a clinical prognostic value for HNSCC. Using immunocompetent transgenic mouse model with spontaneous HNSCC, we directly observed that targeting CTLA4 decreases MDSCs and M2 macrophages and promotes T cell activation in both tumor microenvironment and macro-environment. In all, our study provides direct evidence in vivo and proposes a rationale for CTLA4 inhibition as a future therapeutic strategy in patients with HNSCC.
引用
收藏
页数:12
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