Physiological Genomics, Biomedical Center, Ludwig-Maximilians University Munich, 82152, Planegg/Munich, Germany.
Barbara & Donald Jonas Laboratory of Stem Cells & Regenerative Medicine and Bernard & Shirlee Brown Glaucoma Laboratory, Departments of Pathology and Cell Biology, Columbia University, New York, NY, USA.
Adv Exp Med Biol. 2018;1074:101-107. doi: 10.1007/978-3-319-75402-4_13.
Retinal gene therapy has yet to achieve sustained rescue after disease onset - perhaps because transduction efficiency is insufficient ("too little") and/or the disease is too advanced ("too late") in humans. To test the latter hypothesis, we used a mouse model for retinitis pigmentosa (RP) that allowed us to restore the mutant gene in all diseased rod photoreceptor cells, thereby generating optimally treated retinas. We then treated mice at an advanced disease stage and analyzed the rescue. We showed stable, sustained rescue of photoreceptor structure and function for at least 1 year, demonstrating gene therapy efficacy after onset of degeneration. The results suggest that RP patients are treatable, even when the therapy is administered at late disease stages.
视网膜基因治疗在疾病发作后尚未实现持续的挽救效果——这可能是因为在人类中,转导效率不足(“太少”)和/或疾病过于晚期(“太晚”)。为了验证后一种假设,我们使用了一种视网膜色素变性(RP)的小鼠模型,该模型使我们能够在所有患病的杆状光感受器细胞中恢复突变基因,从而产生最佳治疗的视网膜。然后,我们在疾病晚期对小鼠进行治疗并分析挽救效果。我们发现,光感受器结构和功能至少稳定持续挽救了 1 年,证明了在变性发生后基因治疗的有效性。这些结果表明,即使在疾病晚期进行治疗,RP 患者也是可治疗的。