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Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia

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dc.contributor.author Tigu, Adrian Bogdan
dc.contributor.author Constantinescu, Catalin Sorin
dc.contributor.author Teodorescu, Patric
dc.contributor.author Kegyes, David
dc.contributor.author Munteanu, Raluca
dc.contributor.author Feder, Richard
dc.contributor.author Peters, Mareike
dc.contributor.author Pralea, Ioana
dc.contributor.author Iuga, Cristina
dc.contributor.author Cenariu, Diana
dc.contributor.author Marcu, Andra
dc.contributor.author Tanase, Alina
dc.contributor.author Colita, Anca
dc.contributor.author Drula, Rares
dc.contributor.author Bergþórsson, Jón Þór
dc.contributor.author Greiff, Victor
dc.contributor.author Dima, Delia
dc.contributor.author Selicean, Cristina
dc.contributor.author Rus, Ioana
dc.contributor.author Zdrenghea, Mihnea
dc.contributor.author Gulei, Diana
dc.contributor.author Ghiaur, Gabriel
dc.contributor.author Tomuleasa, Ciprian
dc.date.accessioned 2023-09-07T01:05:19Z
dc.date.available 2023-09-07T01:05:19Z
dc.date.issued 2023-10
dc.identifier.citation Tigu , A B , Constantinescu , C S , Teodorescu , P , Kegyes , D , Munteanu , R , Feder , R , Peters , M , Pralea , I , Iuga , C , Cenariu , D , Marcu , A , Tanase , A , Colita , A , Drula , R , Bergþórsson , J Þ , Greiff , V , Dima , D , Selicean , C , Rus , I , Zdrenghea , M , Gulei , D , Ghiaur , G & Tomuleasa , C 2023 , ' Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia ' , Journal of Cellular and Molecular Medicine , vol. 27 , no. 19 , pp. 2864-2875 . https://doi.org/10.1111/jcmm.17810
dc.identifier.issn 1582-1838
dc.identifier.other 182427000
dc.identifier.other 963b3652-2281-4c51-b0d2-557fd82e4ab3
dc.identifier.other 37667538
dc.identifier.other 85169808579
dc.identifier.other unpaywall: 10.1111/jcmm.17810
dc.identifier.uri https://hdl.handle.net/20.500.11815/4463
dc.description Funding Information: Adrian Bogdan Tigu and Catalin Constantinescu contributed equally to the current manuscript. Catalin Constantinescu is funded by an internal grant of the Iuliu Hatieganu University – School of Doctoral Studies. David Kegyes is funded by an internal grant of the Iuliu Hatieganu University – School of Medicine. Mareike Peters is funded by a national grant of the Romanian Society for Bone Marrow Transplantation. Ciprian Tomuleasa is also supported by a grant awarded by the Romanian National Ministry of Research, Innovation and Digitalization: PN‐III‐P4‐ID‐PCE‐2020‐1118 within PNCDI IV, Projects for Exploratory Medicine; Projects for Exploratory Medicine—PCE 225/2021; as well as a national grant awarded to Young Research Teams (PN‐III‐PI‐1.1‐TE‐2019‐0271 –‘Supporting a team of young researchers to create an independent research program based on the use of Sleeping Beauty protocol f or the development of CAR T Cells – SEATTLE’). Diana Gulei, Diana Cenariu, Adrian Bogdan Tigu, Jon Thor Bergthorsson and Victor Greiff are supported by an international collaborative grant of the European Economic Space between Romania and Iceland 2021–2023: ‘Cooperation strategy for knowledge transfer, internationalization and curricula innovation in the field of research education at the 3rd level of study –AURORA.’ Publisher Copyright: © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.
dc.description.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.
dc.format.extent 12
dc.format.extent 2539137
dc.format.extent 2864-2875
dc.language.iso en
dc.relation.ispartofseries Journal of Cellular and Molecular Medicine; 27(19)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Náttúrufræðingar
dc.subject B cell
dc.subject CAR T cells
dc.subject CRS
dc.subject megakaryoblastic leukaemia
dc.subject Molecular Medicine
dc.subject Cell Biology
dc.title Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1111/jcmm.17810
dc.relation.url http://www.scopus.com/inward/record.url?scp=85169808579&partnerID=8YFLogxK
dc.contributor.department Other departments
dc.contributor.department Faculty of Medicine


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