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Sickle cell disease: understanding pathophysiology, clinical features and advances in gene therapy approaches

Bakhtiar, M. Taher and Aminondin, Sofea 'Aisyah and Nasir, Nur Asyilah and Jasmadi, Noor Afiqah and Nizam, Nur Irdeena Nabella and Shahrul, Ilhan Syahmi and Darnis, Deny Susanti and Khotib, Junaidi and Faiyazuddin, Md and Widodo, Riyanto Teguh and Haris, Muhammad Salahuddin (2025) Sickle cell disease: understanding pathophysiology, clinical features and advances in gene therapy approaches. Frontiers in Pharmacology, 16. pp. 1-15. E-ISSN 1663-9812

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Abstract

Sickle cell disease (SCD) is an inherited blood disorder marked by the production of abnormal hemoglobin, leading to the distortion—or sickling—of red blood cells. The SCD arises from a single-point mutation that substitutes glutamic acid with valine at the sixth codon of the β-globin chain in hemoglobin. This substitution promotes deoxyhemoglobin aggregation, elevating red blood cell stiffness, and triggering vaso-occlusive and hemolytic repercussions. To explore therapeutic advances in tackling this disease, this review analyzed articles published from January 2015 to January 2025 using the three databases using relevant keywords focusing on SCD and advancement in therapy. It was found that allogeneic hematopoietic stem cell (HSC) transplantation can alleviate symptoms but is limited by a shortage of well-matched donors and immunological challenges. In contrast, autologous gene-modified HSC transplantation via gene therapy offers comparable therapeutic benefits without associated immunological complications. Clinical trials utilizing lentiviral vector-mediated gene insertion have demonstrated promising therapeutic outcomes by preventing hemoglobin aggregation. Emerging gene editing approaches such as CRISPR/Cas9 are expanding treatment options, marking the transition of SCD gene therapy from theoretical concept to clinical application.

Item Type: Article (Review)
Additional Information: 5209/122896
Uncontrolled Keywords: anemia, gene therapy, gene editing, CRISPR, hemoglobinopathies, hematopoietic stem, cell transplantation
Subjects: R Medicine > RS Pharmacy and materia medica
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Pharmacy
Kulliyyah of Science
Kulliyyah of Science > Department of Chemistry
Depositing User: Dr Deny Susanti Darnis
Date Deposited: 26 Aug 2025 12:57
Last Modified: 26 Aug 2025 13:04
URI: http://irep.iium.edu.my/id/eprint/122896

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