CD33 Directed Chimeric Antigen Receptor T Cell Therapy As a Novel Preparative Regimen Prior to Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia 

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CD33 Directed Chimeric Antigen Receptor T Cell Therapy As a Novel Preparative Regimen Prior to Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia  Saad S. Kenderian, MD, Marco Ruella, MD, Olga Shestova, PhD, Michael Klichinsky, John Scholler, Decheng Song, David L. Porter, MD, Martin Carroll, MD, Carl H. June, MD, Saar Gill, MBBS, PhD  Biology of Blood and Marrow Transplantation  Volume 21, Issue 2, Pages S25-S26 (February 2015) DOI: 10.1016/j.bbmt.2014.11.013 Copyright © 2015 Terms and Conditions

Figure 1 Leukemic burden and overall survival in primary AML xenografts following treatment with T cells. Primary AML was injected on Day 0 (5xl06) and T cells were injected on day 15 (1x105). Biology of Blood and Marrow Transplantation 2015 21, S25-S26DOI: (10.1016/j.bbmt.2014.11.013) Copyright © 2015 Terms and Conditions

Figure 2 The combination of RNA-CART33 and chemotherapy result in deeper and prolonged response of leukemia in M0LM14 engrafted xenografts. NSG mice were injected with MOLM14-luc(lxl0(6) I.V) and imaged to confirmed engraftment four days later. Mice were then randomized to receive either RNA-CART33 with cyclophosphamide or untransduced T cells with cyclophosphamide (60 mg/kg L.P). T cell were given at a dose if 10x10(6) I.V in three different doses, on days 5,9,16. Cyclophosphamide was given on days 8 and 14. Biology of Blood and Marrow Transplantation 2015 21, S25-S26DOI: (10.1016/j.bbmt.2014.11.013) Copyright © 2015 Terms and Conditions