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

IF 5.3 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology Journal of Cellular and Molecular Medicine Pub Date : 2023-09-04 DOI:10.1111/jcmm.17810
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
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引用次数: 1

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.

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用于治疗急性巨核细胞白血病的抗CD41 CAR T细胞的设计和临床前测试。
急性巨核细胞白血病(AMkL)是一种罕见的急性髓细胞白血病(AML)亚型,占所有报告病例的5%,经常在唐氏综合征儿童中诊断。被诊断为AMkL的患者总体生存率较低,治疗效果较差,因此CAR T细胞治疗等新疗法可能是治疗AMkL中的一种替代方案。我们研究了一种靶向CD41(M7 AMkL的特异性表面抗原)的新CAR T细胞对AMkL体外模型DAMI Luc2细胞系的影响。进行的流式细胞术评估强调了93.8%的CAR T细胞eGFP阳性的百分比,以及降低靶细胞群的有限急性作用。然而,效应细胞和靶细胞(E:T)之间的相互作用,在低比率下,降低了细胞膜的完整性,并在24小时后减少了M7 AMkL细胞群 h,而在具有较高E:T比率的组中细胞毒性作用不显著。我们的研究结果表明,抗CD41 CAR T细胞在有限的时间内是有效的,并且在低E:T比率的所有实验组中都可以看到细胞毒性作用。
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来源期刊
CiteScore
10.00
自引率
1.90%
发文量
496
审稿时长
28 weeks
期刊介绍: Bridging physiology and cellular medicine, and molecular biology and molecular therapeutics, Journal of Cellular and Molecular Medicine publishes basic research that furthers our understanding of the cellular and molecular mechanisms of disease and translational studies that convert this knowledge into therapeutic approaches.
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