San Raffaele Telethon Institute for Gene Therapy, San Raffaele Scientific Institute, Via Olgettina 58, Milan, Italy.
Blood. 2012 Nov 29;120(23):4517-20. doi: 10.1182/blood-2012-05-432591. Epub 2012 Oct 4.
Gene therapy may provide a cure for hemophilia and overcome the limitations of protein replacement therapy. Increasing the potency of gene transfer vectors may allow improvement of their therapeutic index, as lower doses can be administered to achieve therapeutic benefit, reducing toxicity of in vivo administration. Here we generated codon-usage optimized and hyperfunctional factor IX (FIX) transgenes carrying an R338L amino acid substitution (FIX Padua), previously associated with clotting hyperactivity and thrombophilia. We delivered these transgenes to hemophilia B mice by hepatocyte-targeted integration-competent and -defective lentiviral vectors. The hyperfunctional FIX transgenes increased FIX activity reconstituted in the plasma without detectable adverse effects, allowing correction of the disease phenotype at lower vector doses and resulting in improved hemostasis in vivo. The combined effect of codon optimization with the hyperactivating FIX-R338L mutation resulted in a robust 15-fold gain in potency and therefore provides a promising strategy to improve the efficacy, feasibility, and safety of hemophilia gene therapy.
基因治疗可能为血友病提供治愈方法,并克服蛋白质替代疗法的局限性。提高基因转移载体的效力可以改善其治疗指数,因为较低剂量即可实现治疗效果,从而降低体内给药的毒性。在这里,我们生成了经过密码子优化的和超功能的因子 IX(FIX)转基因,携带先前与凝血过度活跃和血栓形成相关的 R338L 氨基酸取代(FIX Padua)。我们通过肝细胞靶向整合有功能和无功能的慢病毒载体将这些转基因递送到血友病 B 小鼠体内。超功能 FIX 转基因增加了血浆中再构成的 FIX 活性,而没有可检测到的不良影响,从而允许在较低的载体剂量下纠正疾病表型,并导致体内止血效果得到改善。密码子优化与超激活 FIX-R338L 突变的联合作用导致效力提高了 15 倍,因此为提高血友病基因治疗的疗效、可行性和安全性提供了有前途的策略。