Cellular and Molecular Therapeutics Branch, National Heart, Lung, and Blood Institute (NHLBI) / National Institute of Diabetes, and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), Bethesda, Maryland, MD, USA.
Division of Molecular and Medical Genetics, Center for Gene and Cell Therapy, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Nat Commun. 2023 Oct 12;14(1):6291. doi: 10.1038/s41467-023-41153-5.
Hematopoietic stem cell (HSC) gene therapy has curative potential; however, its use is limited by the morbidity and mortality associated with current chemotherapy-based conditioning. Targeted conditioning using antibody-drug conjugates (ADC) holds promise for reduced toxicity in HSC gene therapy. Here we test the ability of an antibody-drug conjugate targeting CD117 (CD117-ADC) to enable engraftment in a non-human primate lentiviral gene therapy model of hemoglobinopathies. Following single-dose CD117-ADC, a >99% depletion of bone marrow CD34 + CD90 + CD45RA- cells without lymphocyte reduction is observed, which results are not inferior to multi-day myeloablative busulfan conditioning. CD117-ADC, similarly to busulfan, allows efficient engraftment, gene marking, and vector-derived fetal hemoglobin induction. Importantly, ADC treatment is associated with minimal toxicity, and CD117-ADC-conditioned animals maintain fertility. In contrast, busulfan treatment commonly causes severe toxicities and infertility in humans. Thus, the myeloablative capacity of single-dose CD117-ADC is sufficient for efficient engraftment of gene-modified HSCs while preserving fertility and reducing adverse effects related to toxicity in non-human primates. This targeted conditioning approach thus provides the proof-of-principle to improve risk-benefit ratio in a variety of HSC-based gene therapy products in humans.
造血干细胞 (HSC) 基因治疗具有治愈潜力;然而,由于目前基于化疗的调理相关的发病率和死亡率,其应用受到限制。使用抗体药物偶联物 (ADC) 进行靶向调理有望降低 HSC 基因治疗的毒性。在这里,我们测试了一种针对 CD117 的抗体药物偶联物 (CD117-ADC) 在血红蛋白病的非人类灵长类动物慢病毒基因治疗模型中促进植入的能力。在单次给予 CD117-ADC 后,观察到骨髓 CD34+CD90+CD45RA-细胞的>99%耗竭,而不减少淋巴细胞,其结果并不逊于多日骨髓清除性白消安调理。CD117-ADC 与白消安一样,允许有效植入、基因标记和载体衍生的胎儿血红蛋白诱导。重要的是,ADC 治疗相关的毒性最小,并且 CD117-ADC 调理的动物保持生育能力。相比之下,白消安治疗在人类中通常会引起严重的毒性和不育。因此,单次给予 CD117-ADC 的骨髓清除能力足以有效植入基因修饰的 HSC,同时保留生育能力并降低非人类灵长类动物与毒性相关的不良影响。这种靶向调理方法为改善各种基于 HSC 的基因治疗产品在人类中的风险效益比提供了原理验证。