Recent Advances in the Development of Anti-FLT3 CAR T-Cell Therapies for Treatment of AML

被引:12
作者
Pedersen, Maya Graham [1 ]
Moller, Bjarne Kuno [1 ]
Bak, Rasmus O. [2 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Immunol, DK-8200 Aarhus, Denmark
[2] Aarhus Univ, Dept Biomed, DK-8000 Aarhus, Denmark
基金
欧洲研究理事会;
关键词
FLT3; AML; leukemia; FMS-like tyrosine kinase-3; CAR T; CAR; chimeric antigen receptor; FLT3L; ACUTE MYELOID-LEUKEMIA; INTERNAL TANDEM DUPLICATION; HEMATOPOIETIC STEM-CELL; PROGNOSTIC RELEVANCE; 4-1BB COSTIMULATION; NORMAL CYTOGENETICS; FLT3; GENE; MUTATIONS; TRANSPLANTATION; CHEMOTHERAPY;
D O I
10.3390/biomedicines10102441
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Following the success of the anti-CD19 chimeric antigen receptor (CAR) T-cell therapies against B-cell malignancies, the CAR T-cell approach is being developed towards other malignancies like acute myeloid leukemia (AML). Treatment options for relapsed AML patients are limited, and the upregulation of the FMS-like tyrosine kinase 3 (FLT3) in malignant T-cells is currently not only being investigated as a prognostic factor, but also as a target for new treatment options. In this review, we provide an overview and discuss different approaches of current anti-FLT3 CAR T-cells under development. In general, these therapies are effective both in vitro and in vivo, however the safety profile still needs to be further investigated. The first clinical trials have been initiated, and the community now awaits clinical evaluation of the approach of targeting FLT3 with CAR T-cells.
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页数:15
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