| Literature DB >> 30826931 |
Gina Ma1, Jiaqi Shen1, Kevin Pinz1, Masayuki Wada2, Jino Park3, Soojin Kim3, Tomiteru Togano4, William Tse5,6.
Abstract
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.Entities:
Keywords: Alemtuzumab; Anti-CD4 CAR; CAMPATH; Immunotherapy; T cell malignancies; T-cells
Year: 2019 PMID: 30826931 DOI: 10.1007/s12015-019-09876-5
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 5.739