genetic engineering in hematopoietic stem cells for β-hemoglobinopathies treatment: advances, challenges, and clinical translation

Β-hemoglobinopathies rank among the most prevalent inherited blood disorders globally. traditional management strategies are primarily palliative and often associated with significant challenges, including iron overload and limited long-term efficacy. allogeneic hematopoietic stem cell transplantation (hsct) is a potentially curative option for transfusion-dependent patients, but its broader applicability is constrained by factors that limit its use. utilizing viral vectors and gene-editing tools, particularly crispr-cas9 technology, researchers have developed therapies that target the root causes of these disorders. these innovative approaches have demonstrated substantial therapeutic potential, accompanied by favorable safety profiles, in clinical settings. since the initial investigations, the genome editing tool has rapidly advanced for genetic abnormalities, particularly monogenic blood diseases, including β-hemoglobinopathies. this method suggests an approach with lower concerns in viral gene integration and insertional mutagenesis issues. this review comprehensively surveys the therapeutic strategies for β-thalassemia and sickle cell disease (scd) currently in preclinical and clinical development, with a focus on the evolving treatment paradigm. looking forward, critical research priorities include optimizing the efficiency and specificity of gene-editing platforms and pioneering novel delivery systems to guarantee both therapeutic efficacy and clinical safety.