A cycle involving HMGB1, IFN-γ and dendritic cells plays a putative role in anti-tumor immunity

被引:27
作者
Gao, Qun [1 ,2 ]
Li, Feng [1 ]
Wang, Shumin [1 ]
Shen, Zhibo [1 ]
Chen, Shaoyan [1 ]
Ping, Yu [1 ]
Qin, Guohui [1 ]
Chen, Xinfeng [1 ]
Yang, Li [1 ]
Cao, Ling [1 ]
Liu, Shasha [1 ]
Zhang, Bin [3 ]
Wang, Liping [2 ]
Sun, Yan [5 ]
Zhang, Yi [1 ,2 ,4 ,6 ]
机构
[1] Zhengzhou Univ, Biotherapy Ctr, Affiliated Hosp 1, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ, Canc Ctr, Affiliated Hosp 1, Zhengzhou 450052, Henan, Peoples R China
[3] Northwestern Univ, Sch Med, Dept Hematol Oncol, Chicago, IL USA
[4] Zhengzhou Univ, Sch Life Sci, Zhengzhou 450001, Henan, Peoples R China
[5] Chinese Acad Med Sci, Canc Hosp, Beijing 100021, Peoples R China
[6] Henan Key Lab Tumor Immunol & Biotherapy, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Interferon-gamma; High-mobility group box 1; Dendritic cell; Cytotoxic T lymphocyte; CCL5; CXCL10; CXCL11; CCR5; CXCR3; MOBILITY GROUP BOX-1; RECEPTOR; DIFFERENTIATION; CHEMOTHERAPY; MATURATION; EFFECTOR; DISTINCT; REVEALS; DAMAGE; DEATH;
D O I
10.1016/j.cellimm.2018.08.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An important subset in regulating antitumor immunity is the maturation and accumulation of intratumor dendritic cells (DCs), inducing potent T cell cytotoxicity. In this study, we explored how the soluble abundant high-mobility group box 1 protein (HMGB1) affected DC activation and retention within lung cancers, and in which way the resultant interferon-gamma (IFN-gamma) further enhanced DC maturation and accumulation. It was discovered that HMGB1 was correlated with DC markers HLA-DR and CD86 in lung cancers at both mRNA and protein level. Further analyses showed HMGB1 enhanced the maturation of DCs, indicated by upregulated IFN-gamma in CD8(+) T cells. Additionally, HMGB1 increased the accumulation of DCs by promoting CCR5 and CXCR3 production. Moreover, the resultant IFN-gamma elevated the levels of HMGB1 and DC-associated chemokines, CCL5, CXCL10 and CXCL11 in tumor cells. Hence, the HMGB1-IFN-gamma cycle may represent an important mechanism underlying DC-mediated anti-tumor immune response.
引用
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页数:9
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