Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Mol Ther. 2020 Jul 8;28(7):1684-1695. doi: 10.1016/j.ymthe.2020.04.021. Epub 2020 Apr 29.
There is a strong rationale to consider future cell therapeutic approaches for cystic fibrosis (CF) in which autologous proximal airway basal stem cells, corrected for CFTR mutations, are transplanted into the patient's lungs. We assessed the possibility of editing the CFTR locus in these cells using zinc-finger nucleases and have pursued two approaches. The first, mutation-specific correction, is a footprint-free method replacing the CFTR mutation with corrected sequences. We have applied this approach for correction of ΔF508, demonstrating restoration of mature CFTR protein and function in air-liquid interface cultures established from bulk edited basal cells. The second is targeting integration of a partial CFTR cDNA within an intron of the endogenous CFTR gene, providing correction for all CFTR mutations downstream of the integration and exploiting the native CFTR promoter and chromatin architecture for physiologically relevant expression. Without selection, we observed highly efficient, site-specific targeted integration in basal cells carrying various CFTR mutations and demonstrated restored CFTR function at therapeutically relevant levels. Significantly, Omni-ATAC-seq analysis revealed minimal impact on the positions of open chromatin within the native CFTR locus. These results demonstrate efficient functional correction of CFTR and provide a platform for further ex vivo and in vivo editing.
有充分的理由考虑未来用于囊性纤维化 (CF) 的细胞治疗方法,即将经过 CFTR 突变校正的自体近端气道基底干细胞移植到患者的肺部。我们评估了使用锌指核酸酶编辑这些细胞中 CFTR 基因座的可能性,并采用了两种方法。第一种是特异性突变校正,是一种无痕方法,用校正后的序列替换 CFTR 突变。我们已经应用这种方法校正 ΔF508,证明在从批量编辑的基底细胞建立的气液界面培养物中恢复成熟 CFTR 蛋白和功能。第二种是靶向将部分 CFTR cDNA 整合到内源性 CFTR 基因的内含子中,为整合下游的所有 CFTR 突变提供校正,并利用天然 CFTR 启动子和染色质结构进行生理相关的表达。在没有选择的情况下,我们观察到携带各种 CFTR 突变的基底细胞中高效、特异性的靶向整合,并证明在治疗相关水平恢复 CFTR 功能。重要的是,Omni-ATAC-seq 分析显示对天然 CFTR 基因座中开放染色质位置的影响最小。这些结果证明了 CFTR 的有效功能校正,并为进一步的体外和体内编辑提供了一个平台。