Targeting T Cell Malignancies Using CD4CAR T-Cells and Implementing a Natural Safety Switch

被引:0
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作者
Gina Ma
Jiaqi Shen
Kevin Pinz
Masayuki Wada
Jino Park
Soojin Kim
Tomiteru Togano
William Tse
机构
[1] Long Island High Technology Incubator,iCell Gene Therapeutics LLC, Research & Development Division
[2] University of Louisville,Division of Blood and Bone Marrow Transplantation, James Graham Brown Cancer Center
[3] National Center for Global Health and Medicine,Department of Hematology
[4] University of Louisville School of Medicine,Department of Medicine
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关键词
T-cells; Immunotherapy; T cell malignancies; CAMPATH; Alemtuzumab; Anti-CD4 CAR;
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摘要
T cell malignancies are aggressive diseases with no standard treatment available, often resulting in poor patient outcomes. Lately, the recent FDA approval of a CD19 CAR T cell therapy for B cell acute lymphoblastic leukemia has earned nationwide attention, leading to the possibility that success of CD19 CAR therapy can be extended to T cell malignancies. However, the impact of T cell depletion due to a shared antigen pool remains an issue to be resolved. Here, we describe a CD4CAR capable of eliminating CD4-positive T cell acute lymphoblastic leukemia in a systemic mouse model, with CAMPATH (alemtuzumab) as a natural safety switch to deplete the infused CD4CAR T cells to prevent toxicities associated with CD4 cell aplasia. Our data support the potential use of CD4CAR T cells for the treatment of CD4-postive T-cell acute lymphoblastic leukemia malignancies or refractory disease in clinical settings.
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页码:443 / 447
页数:4
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