CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia.
Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia.
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急性巨核细胞白血病(AMkL)是急性髓系白血病(AML)的罕见亚型,占所有报告病例的 5%,常见于唐氏综合征儿童。AMkL 患者总生存率低、治疗结局较差,因此 CAR-T 细胞疗法等新型疗法可能成为替代治疗方式。本研究在 AMkL 体外模型 DAMI Luc2 细胞系中,评估靶向 M7-AMkL 特异性表面抗原 CD41 的新型 CAR-T 细胞的作用。流式细胞术评估显示,93.8% 的 CAR-T 细胞为 eGFP 阳性,靶细胞群体的急性期降低幅度有限。然而,在低效应细胞/靶细胞(E:T)比例下,效应细胞与靶细胞相互作用降低了细胞膜完整性,并在共培养 24 小时后减少 M7-AMkL 细胞群体;而 E:T 比例较高的组别中,细胞毒作用并不显著。研究结果提示,抗 CD41 CAR-T 细胞的作用时间有限,在所有低 E:T 比例实验组中均可观察到细胞毒作用。
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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