Ethical and regulatory aspects of genome editing.
Donald B KohnMatthew H PorteusAndrew M ScharenbergPublished in: Blood (2016)
Gene editing is a rapidly developing area of biotechnology in which the nucleotide sequence of the genome of living cells is precisely changed. The use of genome-editing technologies to modify various types of blood cells, including hematopoietic stem cells, has emerged as an important field of therapeutic development for hematopoietic disease. Although these technologies offer the potential for generation of transformative therapies for patients suffering from myriad disorders of hematopoiesis, their application for therapeutic modification of primary human cells is still in its infancy. Consequently, development of ethical and regulatory frameworks that ensure their safe and effective use is an increasingly important consideration. Here, we review a number of issues that have the potential to impact the clinical implementation of genome-editing technologies, and suggest paths forward for resolving them such that new therapies can be safely and rapidly translated to the clinic.
Keyphrases
- genome editing
- crispr cas
- living cells
- stem cells
- end stage renal disease
- primary care
- fluorescent probe
- bone marrow
- transcription factor
- chronic kidney disease
- newly diagnosed
- induced apoptosis
- healthcare
- cell cycle arrest
- prognostic factors
- single molecule
- peritoneal dialysis
- cell proliferation
- physical activity
- gene expression
- quality improvement
- human health
- mesenchymal stem cells
- genome wide
- weight loss
- patient reported
- cell therapy
- pi k akt