Low-Dose Gemcitabine Treatment Enhances Immunogenicity and Natural Killer Cell-Driven Tumor Immunity in Lung Cancer

被引:52
|
作者
Zhang, Xin [1 ]
Wang, Dong [2 ]
Li, Zhidong [3 ]
Jiao, Defeng [2 ]
Jin, Linlin [2 ]
Cong, Jingjing [2 ]
Zheng, Xiaohu [2 ]
Xu, Lijun [1 ]
机构
[1] First Hosp Jilin Univ, Dept Resp Med, Changchun, Peoples R China
[2] Univ Sci & Technol China, Sch Life Sci, Div Mol Med, Hefei Natl Lab Phys Sci Microscale,CAS Key Lab In, Hefei, Peoples R China
[3] First Hosp Jilin Univ, Dept Rehabil Med, Changchun, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
low-dose gemcitabine; NK cells; immunogenicity; antitumor immunity; lung cancer; NKG2D LIGANDS; CALRETICULIN EXPOSURE; DANGER SIGNALS; UP-REGULATION; PHASE-III; DEATH; CHEMOTHERAPY; EXPRESSION; CISPLATIN; IMMUNOTHERAPY;
D O I
10.3389/fimmu.2020.00331
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Gemcitabine has been used as first-line chemotherapy against lung cancer, but many patients experience cancer recurrence. Activation of anti-tumor immunity in vivo has become an important way to prevent recurrence. Anti-tumor immune responses are often dependent upon the immunogenicity of tumors. In our study, we observed that low-dose gemcitabine treatment enhanced the immunogenicity of lung cancer by increasing the exposure of calreticulin, high mobility group box 1, and upregulating expression of NKG2D ligands. Further studies demonstrated that low-dose gemcitabine treatment increased interferon-gamma expression and NK-cell activation in mice. Low-dose gemcitabine treatment was sufficient for inhibiting tumor growth with few side effects in vivo. These data suggest that low-dose gemcitabine-induced immunochemotherapy activated antitumor immunity in immunocompetent patients.
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页数:14
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