Phase I trials using Sleeping Beauty to generate CD19-specific CAR T cells

Partow Kebriaei(Cellular Therapeutics (United Kingdom)), Harjeet Singh(Pediatrics and Genetics), M. Helen Huls(Pediatrics and Genetics), Matthew J. Figliola(Pediatrics and Genetics), Roland L. Bassett(The University of Texas MD Anderson Cancer Center), Simon Olivares(Pediatrics and Genetics), Bipulendu Jena(Pediatrics and Genetics), Margaret J. Dawson(Pediatrics and Genetics), Pappanaicken R. Kumaresan(Pediatrics and Genetics), Shihuang Su(Pediatrics and Genetics), Sourindra N. Maiti(Pediatrics and Genetics), Jianliang Dai(The University of Texas MD Anderson Cancer Center), Branden S. Moriarity, Marie-Andrée Forget(Pediatrics and Genetics), Vladimir Senyukov(Pediatrics and Genetics), Aaron Orozco(Pediatrics and Genetics), Tingting Liu(Cellular Therapeutics (United Kingdom)), Jessica M McCarty(Cellular Therapeutics (United Kingdom)), Rineka N. Jackson(Pediatrics and Genetics), Judy S. Moyes(Pediatrics and Genetics), Gabriela Rondón(Cellular Therapeutics (United Kingdom)), Muzaffar H. Qazilbash(Cellular Therapeutics (United Kingdom)), Stefan O. Ciurea(Cellular Therapeutics (United Kingdom)), Amin M. Alousi(Cellular Therapeutics (United Kingdom)), Yago Nieto(Cellular Therapeutics (United Kingdom)), Katy Rezvani(Cellular Therapeutics (United Kingdom)), David Marín(Cellular Therapeutics (United Kingdom)), Uday Popat(Cellular Therapeutics (United Kingdom)), Chitra Hosing(Cellular Therapeutics (United Kingdom)), Elizabeth J. Shpall(Cellular Therapeutics (United Kingdom)), Hagop M. Kantarjian(The University of Texas MD Anderson Cancer Center), Michael J. Keating(The University of Texas MD Anderson Cancer Center), William G. Wierda(The University of Texas MD Anderson Cancer Center), Kim‐Anh Do(The University of Texas MD Anderson Cancer Center), David A. Largaespada, Dean A. Lee(Pediatrics and Genetics), Perry B. Hackett, Richard E. Champlin(Cellular Therapeutics (United Kingdom)), Laurence J.N. Cooper(Pediatrics and Genetics)
Journal of Clinical Investigation
August 1, 2016
Cited by 500Open Access
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Abstract

BACKGROUND: T cells expressing antigen-specific chimeric antigen receptors (CARs) improve outcomes for CD19-expressing B cell malignancies. We evaluated a human application of T cells that were genetically modified using the Sleeping Beauty (SB) transposon/transposase system to express a CD19-specific CAR. METHODS: T cells were genetically modified using DNA plasmids from the SB platform to stably express a second-generation CD19-specific CAR and selectively propagated ex vivo with activating and propagating cells (AaPCs) and cytokines. Twenty-six patients with advanced non-Hodgkin lymphoma and acute lymphoblastic leukemia safely underwent hematopoietic stem cell transplantation (HSCT) and infusion of CAR T cells as adjuvant therapy in the autologous (n = 7) or allogeneic settings (n = 19). RESULTS: SB-mediated genetic transposition and stimulation resulted in 2,200- to 2,500-fold ex vivo expansion of genetically modified T cells, with 84% CAR expression, and without integration hotspots. Following autologous HSCT, the 30-month progression-free and overall survivals were 83% and 100%, respectively. After allogeneic HSCT, the respective 12-month rates were 53% and 63%. No acute or late toxicities and no exacerbation of graft-versus-host disease were observed. Despite a low antigen burden and unsupportive recipient cytokine environment, CAR T cells persisted for an average of 201 days for autologous recipients and 51 days for allogeneic recipients. CONCLUSIONS: CD19-specific CAR T cells generated with SB and AaPC platforms were safe, and may provide additional cancer control as planned infusions after HSCT. These results support further clinical development of this nonviral gene therapy approach. TRIAL REGISTRATION: Autologous, NCT00968760; allogeneic, NCT01497184; long-term follow-up, NCT01492036. FUNDING: National Cancer Institute, private foundations, and institutional funds. Please see Acknowledgments for details.


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