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Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia
Authors:Adrian Bogdan Tigu  Catalin Sorin Constantinescu  Patric Teodorescu  David Kegyes  Raluca Munteanu  Richard Feder  Mareike Peters  Ioana Pralea  Cristina Iuga  Diana Cenariu  Andra Marcu  Alina Tanase  Anca Colita  Rares Drula  Jon Thor Bergthorsson  Victor Greiff  Delia Dima  Cristina Selicean  Ioana Rus  Mihnea Zdrenghea  Diana Gulei  Gabriel Ghiaur  Ciprian Tomuleasa
Institution:1. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Contribution: Formal analysis (equal), ​Investigation (equal);2. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Department of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Intensive Care Unit, Emergency Clinical Hospital, Cluj-Napoca, Romania

Contribution: Data curation (equal), Formal analysis (equal);3. Department of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Department of Leukemia, Sidney Kimmel Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

Contribution: ​Investigation (equal);4. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Department of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Contribution: ​Investigation (equal);5. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Contribution: ​Investigation (equal);6. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Department of Drug Analysis, School of Pharmacy, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Contribution: ​Investigation (equal);7. Department of Pediatrics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

Department of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania

Contribution: ​Investigation (equal);8. Stem Cell Research Unit, Biomedical Center, School of Health Sciences, University of Iceland, Reykjavík, Iceland

Department of Laboratory Hematology, Landspitali University Hospital, Reykjavík, Iceland

Contribution: ​Investigation (equal);9. Department of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway

Contribution: Conceptualization (equal);10. Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania

Contribution: ​Investigation (equal);11. Department of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania

Contribution: Formal analysis (equal);12. Medfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania

Abstract:Acute megakaryoblastic leukaemia (AMkL) is a rare subtype of acute myeloid leukaemia (AML) representing 5% of all reported cases, and frequently diagnosed in children with Down syndrome. Patients diagnosed with AMkL have low overall survival and have poor outcome to treatment, thus novel therapies such as CAR T cell therapy could represent an alternative in treating AMkL. We investigated the effect of a new CAR T cell which targets CD41, a specific surface antigen for M7-AMkL, against an in vitro model for AMkL, DAMI Luc2 cell line. The performed flow cytometry evaluation highlighted a percentage of 93.8% CAR T cells eGFP-positive and a limited acute effect on lowering the target cell population. However, the interaction between effector and target (E:T) cells, at a low ratio, lowered the cell membrane integrity, and reduced the M7-AMkL cell population after 24 h of co-culture, while the cytotoxic effect was not significant in groups with higher E:T ratio. Our findings suggest that the anti-CD41 CAR T cells are efficient for a limited time spawn and the cytotoxic effect is visible in all experimental groups with low E:T ratio.
Keywords:B cell  CAR T cells  CRS  megakaryoblastic leukaemia
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