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铁蛋白聚集细胞衔接器用于 CAR-T 亲和力工程以对抗难治性白血病

英文原题:Ferritin aggregation cell engager for CAR T avidity engineering against refractory leukemias.

查看英文原题

Ferritin aggregation cell engager for CAR T avidity engineering against refractory leukemias.

PubMed 2026/03/09(内容时间) Cell Q1 · IF 45.1(JCR 2025)

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中文摘要

尽管CAR-T(CAR-T)细胞疗法在治疗白血病方面前景广阔,但仍面临导致耐药的关键挑战——抗原调变。基于我们的临床发现,即多种类型的白血病细胞及相应的 CAR-T 细胞均强表达 CD71(一种铁蛋白受体),我们设计了一种铁蛋白聚集细胞衔接器(FACE),其可锚定至 CAR-T 细胞表面,引导 CAR-T 细胞面向白血病细胞,并促进 CAR 对同源抗原的识别。使用多种白血病患者来源细胞和白血病患者来源异种移植模型进行的体外和体内实验表明,我们的 FACE-CAR-T 细胞成功增强了治疗效果且具有良好的生物安全性,降低了克服抗原调变所需的抗原阈值,甚至可将化疗药物装载到铁蛋白中以进行联合治疗。这种亲合力工程为改善 CAR-T 细胞疗法对多种难治性白血病的疗效提供了一种新型、简便、通用且灵活的方法。

展开英文摘要原文

Although promising, chimeric antigen receptor T (CAR T) cell therapy for treating leukemias still faces the critical challenge of antigen modulation, which causes resistance. Building from our clinical insight that both diverse types of leukemia cells and corresponding CAR T cells strongly express CD71 (a ferritin receptor), we designed a ferritin aggregation cell engager (FACE) that can anchor to the CAR T cell surface, guide CAR T cells to face leukemia cells, and facilitate CAR recognition of cognate antigens.

In vitro and in vivo experiments with diverse leukemia patient-derived cells and leukemia patient-derived xenograft models show that our FACE-CAR T cells succeed in enhancing therapeutic efficacy with good biosafety, lowering the antigen threshold for overcoming antigen modulation, and even loading chemodrugs in ferritin for combination therapy. This avidity engineering provides a neotype, facile, universal, and flexible approach for improving the efficacy of CAR T cell therapy for diverse refractory leukemias.

论文信息

作者
Li F、Hu Y、Wang Y、Zhang X、Qiu S、Hu X、Wang W、Wang S
第一作者单位
State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, P.R. China; State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, P.R. China.China
通讯作者单位
State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, P.R. China; State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, P.R. China; School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing, P.R. China. Electronic address: weiwei@ipe.ac.cn.China
期刊
Cell2026 Apr 2
原文标识
PubMed 41806835 · DOI 10.1016/j.cell.2026.02.005