Advancements in Hematopoietic Stem Cell Gene Therapy: A Journey of Progress for Viral Transduction.
Cells
; 13(12)2024 Jun 15.
Article
de En
| MEDLINE
| ID: mdl-38920667
ABSTRACT
Hematopoietic stem cell (HSC) transduction has undergone remarkable advancements in recent years, revolutionizing the landscape of gene therapy specifically for inherited hematologic disorders. The evolution of viral vector-based transduction technologies, including retroviral and lentiviral vectors, has significantly enhanced the efficiency and specificity of gene delivery to HSCs. Additionally, the emergence of small molecules acting as transduction enhancers has addressed critical barriers in HSC transduction, unlocking new possibilities for therapeutic intervention. Furthermore, the advent of gene editing technologies, notably CRISPR-Cas9, has empowered precise genome modification in HSCs, paving the way for targeted gene correction. These striking progresses have led to the clinical approval of medicinal products based on engineered HSCs with impressive therapeutic benefits for patients. This review provides a comprehensive overview of the collective progress in HSC transduction via viral vectors for gene therapy with a specific focus on transduction enhancers, highlighting the latest key developments, challenges, and future directions towards personalized and curative treatments.
Mots clés
Texte intégral:
1
Collection:
01-internacional
Base de données:
MEDLINE
Sujet principal:
Transduction génétique
/
Cellules souches hématopoïétiques
/
Thérapie génétique
/
Vecteurs génétiques
Limites:
Animals
/
Humans
Langue:
En
Journal:
Cells
Année:
2024
Type de document:
Article
Pays d'affiliation:
Allemagne