Induced Pluripotent Stem Cells (iPSCs) and Gene Therapy: A New Era for the Treatment of Neurological Diseases.
Giulia Paolini SguazziValentina MutoTartaglia MarcoEnrico BertiniClaudia CompagnucciPublished in: International journal of molecular sciences (2021)
To date, gene therapy has employed viral vectors to deliver therapeutic genes. However, recent progress in molecular and cell biology has revolutionized the field of stem cells and gene therapy. A few years ago, clinical trials started using stem cell replacement therapy, and the induced pluripotent stem cells (iPSCs) technology combined with CRISPR-Cas9 gene editing has launched a new era in gene therapy for the treatment of neurological disorders. Here, we summarize the latest findings in this research field and discuss their clinical applications, emphasizing the relevance of recent studies in the development of innovative stem cell and gene editing therapeutic approaches. Even though tumorigenicity and immunogenicity are existing hurdles, we report how recent progress has tackled them, making engineered stem cell transplantation therapy a realistic option.
Keyphrases
- gene therapy
- stem cells
- induced pluripotent stem cells
- replacement therapy
- stem cell transplantation
- crispr cas
- clinical trial
- cell therapy
- smoking cessation
- genome editing
- single cell
- randomized controlled trial
- genome wide identification
- copy number
- combination therapy
- transcription factor
- study protocol
- subarachnoid hemorrhage
- single molecule
- case control
- genome wide analysis