Making CAR T Cells a Solid Option for Solid Tumors

被引:142
|
作者
Schmidts, Andrea [1 ]
Maus, Marcela V. [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Canc, Cellular Immunotherapy Program, Boston, MA 02115 USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
immunotherapy; CAR-T cells; solid tumors; cancer; toxicity; cell engineering; CHIMERIC ANTIGEN RECEPTOR; ANTITUMOR-ACTIVITY; ADOPTIVE IMMUNOTHERAPY; CYTOKINE RELEASE; GENE-THERAPY; CANCER; ACTIVATION; AUGMENTS; DELIVERY; HER2;
D O I
10.3389/fimmu.2018.02593
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adoptive cell therapy with chimeric antigen receptor (CAR) T cells aims to redirect the patient's own immune system to selectively attack cancer cells. To do so, CAR T cells are endowed with specific antigen recognition moieties fused to signaling and costimulatory domains. While this approach has shown great success for the treatment of B cell malignancies, response rates among patients with solid cancers are less favorable. The major challenges for CAR T cell immunotherapy in solid cancers are the identification of unique tumor target antigens, as well as improving CAR T cell trafficking to and expansion at the tumor site. This review focuses on combinatorial antigen targeting, regional delivery and approaches to improve CAR T cell persistence in the face of a hostile tumor microenvironment.
引用
收藏
页数:10
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