Podoplanin as an Attractive Target of CAR T Cell Therapy

被引:8
|
作者
Waseda, Masazumi [1 ]
Kaneko, Shin [1 ]
机构
[1] Kyoto Univ, Ctr iPS Cell Res & Applicat CiRA, Dept Cell Growth & Differentiat, Shin Kaneko Lab, Kyoto 6068507, Japan
基金
日本学术振兴会;
关键词
T cell immunotherapy; tumor-specific antigen; chimeric antigen receptor (CAR); cancer-specific monoclonal antibody (CasMab); induced pluripotent stem (iPS) cell; FIBROBLAST ACTIVATION PROTEIN; AGGREGATION-INDUCING FACTOR; CYTOKINE RELEASE SYNDROME; ANTITUMOR-ACTIVITY; CHIMERIC RECEPTORS; ADOPTIVE IMMUNOTHERAPY; METASTATIC MELANOMA; EXPRESSION; CD19; COSTIMULATION;
D O I
10.3390/cells9091971
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To date, various kinds of cancer immunotherapy methods have been developed, but T cell immunotherapy is one of the most promising strategies. In general, T cell receptor (TCR) or chimeric antigen receptor (CAR) is used to modify the antigen specificity of T cells. CARs possess an underlying potential with treatment efficacy to treat a broad range of cancer patients compared with TCRs. Although a variety of CAR molecules have been developed so far, the clinical application for solid tumors is limited partly due to its adverse effect known as "on-target off-tumor toxicity". Therefore, it is very important for CAR T cell therapy to target specific antigens exclusively expressed by malignant cells. Here, we review the application of T cell immunotherapy using specific antigen receptor molecules and discuss the possibility of the clinical application of podoplanin-targeted CAR derived from a cancer-specific monoclonal antibody (CasMab).
引用
收藏
页码:1 / 14
页数:14
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