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Novel Approaches to Enhance the Specificity and Safety of Engineered T Cells
被引:29
|作者:
Fedorov, Victor D.
[1
,2
]
Sadelain, Michel
[1
,3
]
Kloss, Christopher C.
[1
,4
]
机构:
[1] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, New York, NY 10065 USA
[2] Rockefeller Univ, Weill Cornell Med Coll, Triinst MSTP Program, MSKCC, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, New York, NY 10065 USA
[4] Weill Cornell Med Coll, Dept Med Genet, New York, NY USA
来源:
关键词:
T-cell therapies;
cancer immunotherapy;
CD19;
CAR therapies;
SUICIDE GENE-THERAPY;
ADOPTIVE IMMUNOTHERAPY;
CANCER REGRESSION;
CO-STIMULATION;
TOXICITY;
TUMORS;
LYMPHOCYTES;
ACTIVATION;
EXPRESSION;
TARGET;
D O I:
10.1097/PPO.0000000000000040
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
T-cell therapies using engineered T cells show great promise for cancer immunotherapy, as illustrated by the CD19 paradigm. Much of the excitement about this approach, and second-generation CARs in particular, is due to the dramatic clinical results recently reported by a few centers, especially in acute lymphoblastic leukemia, and the applicability of this approach, in principle, to a wide range of cancers. Extending the use of CAR therapies to cancers other than B-cell malignancies will require selective tumor targeting with minimal or acceptable "on-target, off-tumor" effects. The identification of new CAR target antigens is thus one of the next big challenges to address. Recognizing the paucity of currently available tumor-specific targets, we have developed broadly applicable approaches to enhance the tumor selectivity and safety of engineered T cells. Here, we review 2 promising concepts. One is to improve tumor targeting based on combinatorial antigen recognition. The other uses receptors that provide antigen-specific inhibition, which we named iCARs, to divert T cells from the normal tissues one wants to protect.
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页码:160 / 165
页数:6
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