Improving therapy of chronic lymphocytic leukemia with chimeric antigen receptor T cells

被引:10
作者
Fraietta, Joseph A. [1 ]
Schwab, Robert D. [1 ]
Maus, Marcela V. [2 ]
机构
[1] Univ Penn, Ctr Cellular Immunotherapy, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Cellular Immunotherapy Program, Boston, MA USA
关键词
CAR; CLL; Immunotherapy; T cell; Leukemia; ACUTE MYELOID-LEUKEMIA; GROWTH-FACTOR-BETA; ADOPTIVE TRANSFER; B-CELLS; ANTITUMOR-ACTIVITY; SUSTAINED REMISSIONS; CD28; COSTIMULATION; DENDRITIC CELLS; VIVO EXPANSION; GENE-THERAPY;
D O I
10.1053/j.seminoncol.2016.02.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adoptive cell immunotherapy for the treatment of chronic lymphocytic leukemia (CLL) has heralded a new era of synthetic biology. The infusion of genetically engineered, autologous chimeric antigen receptor (CAR) T cells directed against CD19 expressed by normal and malignant B cells represents a novel approach to cancer therapy. The results of recent clinical trials of CAR T cells in relapsed and refractory CLL have demonstrated long-term disease-free remissions, underscoring the power of harnessing and redirecting the immune system against cancer. This review will briefly summarize T-cell therapies in development for CLL disease. We discuss the role of T-cell function and phenotype, T-cell culture optimization, CAR design, and approaches to potentiate the survival and anti-tumor effects of infused lymphocytes. Future efforts will focus on improving the efficacy of CAR T cells for the treatment of CLL and incorporating adoptive cell immunotherapy into standard medical management of CLL. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 299
页数:9
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