Uchida Naoya, Drysdale Claire M, Nassehi Tina, Gamer Jackson, Yapundich Morgan, DiNicola Julia, Shibata Yoshitaka, Hinds Malikiya, Gudmundsdottir Bjorg, Haro-Mora Juan J, Demirci Selami, Tisdale John F
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, MD, USA.
Division of Molecular and Medical Genetics, Center for Gene and Cell Therapy, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo, Japan.
Mol Ther Methods Clin Dev. 2021 Mar 3;21:121-132. doi: 10.1016/j.omtm.2021.02.022. eCollection 2021 Jun 11.
Gene editing with the CRISPR-Cas9 system could revolutionize hematopoietic stem cell (HSC)-targeted gene therapy for hereditary diseases, including sickle cell disease (SCD). Conventional delivery of editing tools by electroporation limits HSC fitness due to its toxicity; therefore, efficient and non-toxic delivery remains crucial. Integrating lentiviral vectors are established for therapeutic gene delivery to engraftable HSCs in gene therapy trials; however, their sustained expression and size limitation preclude their use for CRISPR-Cas9 delivery. Here, we developed a Cas9 protein delivery non-integrating lentiviral system encoding guide RNA and donor DNA, allowing for transient endonuclease function and inclusion of all editing tools in a single vector (all-in-one). We demonstrated efficient one-time correction of the SCD mutation in the endogenous βs-globin gene up to 42% at the protein level (p < 0.01) with the Cas9 protein delivery non-integrating lentiviral all-in-one system without electroporation. Our findings improve prospects for efficient and safe genome editing.
使用CRISPR-Cas9系统进行基因编辑可能会彻底改变针对包括镰状细胞病(SCD)在内的遗传性疾病的造血干细胞(HSC)靶向基因治疗。由于其毒性,通过电穿孔常规递送编辑工具会限制HSC的适应性;因此,高效且无毒的递送仍然至关重要。在基因治疗试验中,整合慢病毒载体已被确立用于将治疗性基因递送至可移植的HSC;然而,它们的持续表达和大小限制使其无法用于CRISPR-Cas9递送。在此,我们开发了一种编码引导RNA和供体DNA的Cas9蛋白递送非整合慢病毒系统,允许瞬时核酸内切酶功能,并将所有编辑工具包含在单个载体中(一体化)。我们证明,使用Cas9蛋白递送非整合慢病毒一体化系统,无需电穿孔,在内源性βs-珠蛋白基因中,SCD突变在蛋白水平上的一次性有效校正率高达42%(p < 0.01)。我们的研究结果改善了高效且安全的基因组编辑的前景。