Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma

被引:53
|
作者
Wang, Yitian [1 ,2 ]
Yu, Wei [1 ,2 ]
Zhu, Jian [1 ,2 ]
Wang, Junjie [1 ,2 ]
Xia, Kaishun [1 ,2 ]
Liang, Chengzhen [1 ,2 ]
Tao, Huimin [1 ,2 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Orthoped, 88 Jie Fang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Orthoped Res Inst, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CAR-T; CD166; 4-1BB; Osteosarcoma; Immunotherapy; PROSTATE-CANCER; COSTIMULATION; DELIVERY; CD6;
D O I
10.1186/s13046-019-1147-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundChimeric antigen receptor (CAR)-engineered T cells have displayed outstanding performance in the treatment of patients with hematological malignancies. However, their efficacy against solid tumors has been largely limited.MethodsIn this study, human osteosarcoma cell lines were prepared, flow cytometry using antibodies against CD166 was performed on different cell samples. CD166-specific T cells were obtained by viral gene transfer of corresponding DNA plasmids and selectively expanded using IL-2 and IL-15. The ability of CD166.BB CAR-T cells to kill CD166(+) osteosarcoma cells was evaluated in vitro and in vivo.ResultsCD166 was selectively expressed on four different human osteosarcoma cell lines, indicating its role as the novel target for CAR-T cell therapy. CD166.BB CAR-T cells killed osteosarcoma cell lines in vitro; the cytotoxicity correlated with the level of CD166 expression on the tumor cells. Intravenous injection of CD166.BB CAR-T cells into mice resulted in the regression of the tumor with no obvious toxicity.ConclusionsTogether, the data suggest that CD166.BB CAR-T cells may serve as a new therapeutic strategy in the future clinical practice for the treatment of osteosarcoma.
引用
收藏
页数:11
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