Next-Generation CAR T-cell Therapies

被引:79
|
作者
Young, Regina M. [1 ,2 ]
Engel, Nils W. [1 ]
Uslu, Ugur [1 ]
Wellhausen, Nils [1 ]
June, Carl H. [1 ,2 ,3 ]
机构
[1] Univ Penn, Perelman Sch Med, Ctr Cellular Immunotherapies, Dept Pathol & Lab Med, Philadelphia, PA USA
[2] Univ Penn, Parker Inst Canc Immunotherapy, Philadelphia, PA USA
[3] Univ Penn, 3400 Civ Ctr Blvd, Philadelphia, PA 19104 USA
关键词
PHASE-1; DOSE-ESCALATION; NATURAL-KILLER-CELLS; IN-VIVO; IMMUNOTHERAPY; EXHIBIT; NK; GLIOBLASTOMA; DYSFUNCTION; EFFICACY; TARGET;
D O I
10.1158/2159-8290.CD-21-1683
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD19-and B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cells have enabled unprecedented responses in a subset of refractory patients with B-cell and plasma cell malignancies, lead-ing to their approval by the FDA for the treatment of leukemia, lymphoma, and myeloma. These "living drugs" can become part of a synthetic immune system, persisting at least a decade in some patients. However, despite this tre-mendous impact, significant unmet treatment needs remain for patients with hematologic malignancies and solid cancers. In this perspective, we highlight recent innovations that advance the field toward production of a more potent and universal cellular immunotherapy of the future. Next-generation CAR T cells will incorporate advances in gene engineering and synthetic biology to enhance functionality and persistence, and reduce treatment-associated toxicities. The combination of autologous CAR T cells with various allogeneic cell treatment strategies designed to target the immunosuppressive tumor microenvironment will broaden the impact of future CAR T-cell therapies.
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页码:1625 / 1633
页数:9
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