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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.
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