| Literature DB >> 27820943 |
Daniel P Dever1, Rasmus O Bak1, Andreas Reinisch2, Joab Camarena1, Gabriel Washington1, Carmencita E Nicolas1, Mara Pavel-Dinu1, Nivi Saxena1, Alec B Wilkens1, Sruthi Mantri1, Nobuko Uchida3, Ayal Hendel1, Anupama Narla4, Ravindra Majeti2, Kenneth I Weinberg1, Matthew H Porteus1.
Abstract
The β-haemoglobinopathies, such as sickle cell disease and β-thalassaemia, are caused by mutations in the β-globin (HBB) gene and affect millions of people worldwide. Ex vivo gene correction in patient-derived haematopoietic stem cells followed by autologous transplantation could be used to cure β-haemoglobinopathies. Here we present a CRISPR/Cas9 gene-editing system that combines Cas9 ribonucleoproteins and adeno-associated viral vector delivery of a homologous donor to achieve homologous recombination at the HBB gene in haematopoietic stem cells. Notably, we devise an enrichment model to purify a population of haematopoietic stem and progenitor cells with more than 90% targeted integration. We also show efficient correction of the Glu6Val mutation responsible for sickle cell disease by using patient-derived stem and progenitor cells that, after differentiation into erythrocytes, express adult β-globin (HbA) messenger RNA, which confirms intact transcriptional regulation of edited HBB alleles. Collectively, these preclinical studies outline a CRISPR-based methodology for targeting haematopoietic stem cells by homologous recombination at the HBB locus to advance the development of next-generation therapies for β-haemoglobinopathies.Entities:
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Year: 2016 PMID: 27820943 PMCID: PMC5898607 DOI: 10.1038/nature20134
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962