通过基因编辑的 CAR T 细胞靶向 CD45,用于白血病根除和造血干细胞移植预处理

Valeria M. Stepanova, Dmitry V. Volkov, Daria S. Osipova, Wenjian Wang, Yingqin Hou, Dmitry E. Pershin, Mariia S. Fadeeva, Ekaterina A. Malakhova, Elena A. Kulakovskaya, Lui Cuicui, Zhao Mingfeng, Hongkai Zhang, Jia Xie, Ding Zhang, Ilgar Z. Mamedov, Alexandr S. Chernov, Georgij B. Telegin, Yuri P. Rubtsov, Alexander G. Gabibov, Peng Wu, Michael A. Maschan, Alexey V. Stepanov
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引用次数: 0

摘要

造血干细胞移植(HSCT)被广泛用于治疗危及生命的血液和免疫系统疾病患者。目前的非靶向化疗/放疗调理方案会造成组织损伤,引起一系列直接和延迟的不良反应,限制了这种救命疗法的应用。替代传统调理方案的需求日益增长,导致了抗体-药物共轭物、裸抗体和 CAR T 细胞等替代方法的开发。在这里,我们介绍一种利用 CAR45 T 细胞靶向造血细胞 CD45 的预处理策略。为了避免CD45 CAR T细胞的自相残杀,我们对人类CD45 CAR T细胞的CD45基因进行了基因组破坏,并结合信号激酶抑制剂达沙替尼。CD45 CAR45 T细胞显示出很强的细胞毒性,并能清除肿瘤细胞。这些细胞能有效地清除人源造血干细胞(HSCs)输注到人源化免疫缺陷小鼠体内的造血细胞。同样,CD45 CAR45 自然杀伤(NK)细胞对肿瘤细胞系和人类造血细胞表现出强大的细胞毒性。因此,我们提供了抗自相残杀的 CAR45 T 细胞和 NK 细胞针对表达 CD45 的肿瘤和造血细胞的生成和临床前疗效的概念证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting CD45 by gene-edited CAR T cells for leukemia eradication and hematopoietic stem cell transplantation preconditioning
Hematopoietic stem cell transplantation (HSCT) is widely used to treat patients with life-threatening hematologic and immune system disorders. Current nontargeted chemo-/radiotherapy conditioning regimens cause tissue injury and induce an array of immediate and delayed adverse effects, limiting the application of this life-saving treatment. The growing demand to replace canonical conditioning regimens has led to the development of alternative approaches, such as antibody-drug conjugates, naked antibodies, and CAR T cells. Here, we introduce a preconditioning strategy targeting CD45 on hematopoietic cells with CAR45 T cells. To avoid fratricide of CD45 CAR T cells, genomic disruption of the CD45 gene was performed on human CD45 CAR T cells in combination with the signaling kinase inhibitor dasatinib. CD45 CAR45 T cells showed high cytotoxicity and depletion of tumor cells These cells were effective in elimination of human hematopoietic cells engrafted in humanized immunodeficient mice by transfusion with human blood-derived hematopoietic stem cells (HSCs). Similarly, CD45 CAR45 natural killer (NK) cells exhibited potent cytotoxicity toward tumor cell lines and human hematopoietic cells . Thus, we provide the proof of concept for the generation and preclinical efficacy of fratricide-resistant CAR45 T and NK cells directed against CD45-expressing tumors and hematopoietic cells.
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