Current approaches to increase CAR T cell potency in solid tumors: targeting the tumor microenvironment

被引:148
作者
Scarfo, Irene
Maus, Marcela V. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Cellular Immunotherapy Program, Ctr Canc, 149 13th St,Room 7-219, Boston, MA 02129 USA
[2] Harvard Med Sch, 149 13th St,Room 7-219, Boston, MA 02129 USA
关键词
Chimeric antigen receptor T-cells; Adoptive immunotherapy; Tumor microenvironment; FIBROBLAST ACTIVATION PROTEIN; CHIMERIC ANTIGEN RECEPTORS; CHECKPOINT BLOCKADE; ANTITUMOR EFFICACY; IL-12; INTERLEUKIN-12; INFILTRATION; TRAFFICKING; RECOGNITION; ERADICATION;
D O I
10.1186/s40425-017-0230-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptor (CAR) T-cell therapy represents a revolutionary treatment for haematological malignancies (i.e. B-ALL). However, the success of this type of treatment has not yet been achieved in solid tumors. One hypothesis is that the immunosuppressive nature of the tumor microenvironment (TME) influences and affects the efficacy of adoptive immunotherapy. Understanding the role of the TME and its interaction with CAR T-cells is crucial to improve the potency of adoptive immunotherapy. In this review, we discuss the strategies and potential combinatorial approaches recently developed in mouse models to enhance the efficacy of CAR T-cells, with particular emphasis on the translational potential of these approaches.
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页数:8
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