Division of Hematopoietic Innovative Therapies, CIEMAT, Madrid, Spain.
Instituto Nacional de Investigación Biomédica en Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
JCI Insight. 2024 May 22;9(10):e171650. doi: 10.1172/jci.insight.171650.
This study lays the groundwork for future lentivirus-mediated gene therapy in patients with Diamond Blackfan anemia (DBA) caused by mutations in ribosomal protein S19 (RPS19), showing evidence of a new safe and effective therapy. The data show that, unlike patients with Fanconi anemia (FA), the hematopoietic stem cell (HSC) reservoir of patients with DBA was not significantly reduced, suggesting that collection of these cells should not constitute a remarkable restriction for DBA gene therapy. Subsequently, 2 clinically applicable lentiviral vectors were developed. In the former lentiviral vector, PGK.CoRPS19 LV, a codon-optimized version of RPS19 was driven by the phosphoglycerate kinase promoter (PGK) already used in different gene therapy trials, including FA gene therapy. In the latter one, EF1α.CoRPS19 LV, RPS19 expression was driven by the elongation factor alpha short promoter, EF1α(s). Preclinical experiments showed that transduction of DBA patient CD34+ cells with the PGK.CoRPS19 LV restored erythroid differentiation, and demonstrated the long-term repopulating properties of corrected DBA CD34+ cells, providing evidence of improved erythroid maturation. Concomitantly, long-term restoration of ribosomal biogenesis was verified using a potentially novel method applicable to patients' blood cells, based on ribosomal RNA methylation analyses. Finally, in vivo safety studies and proviral insertion site analyses showed that lentivirus-mediated gene therapy was nontoxic.
这项研究为未来因核糖体蛋白 S19(RPS19)突变导致的 Diamond Blackfan 贫血(DBA)患者的慢病毒介导基因治疗奠定了基础,显示出一种新的安全有效的治疗方法。数据表明,与范可尼贫血(FA)患者不同,DBA 患者的造血干细胞(HSC)库没有明显减少,这表明收集这些细胞不应该成为 DBA 基因治疗的显著限制。随后,开发了两种临床适用的慢病毒载体。在前一种慢病毒载体 PGK.CoRPS19 LV 中,RPS19 的密码子优化版本由已在不同基因治疗试验中使用的磷酸甘油酸激酶启动子(PGK)驱动,包括 FA 基因治疗。在后一种载体 EF1α.CoRPS19 LV 中,RPS19 的表达由延伸因子 alpha 短启动子 EF1α(s)驱动。临床前实验表明,用 PGK.CoRPS19 LV 转导 DBA 患者的 CD34+细胞可恢复红系分化,并证明了纠正的 DBA CD34+细胞的长期重编程特性,为改善红细胞成熟提供了证据。同时,基于核糖体 RNA 甲基化分析,使用一种可能适用于患者血细胞的新方法,验证了核糖体生物发生的长期恢复。最后,体内安全性研究和前病毒插入位点分析表明,慢病毒介导的基因治疗是无毒的。