Submit manuscript...
Journal of
eISSN: 2475-5540

Stem Cell Research & Therapeutics

Review Article Volume 6 Issue 1

Stem cells in the treatment of sickle cell disease  

Vincent S Gallicchio, Emily McGill

Department of Biological Sciences, College of Science, Clemson University, USA

Received: February 12, 2020 | Published: February 17, 2020

Citation: McGill E, Gallicchio VS. Stem cells in the treatment of sickle cell disease. J Stem Cell Res Ther. 2020;6(1):32?39. DOI: 10.15406/jsrt.2020.06.00138

Download PDF

Abstract

Sickle Cell Disease (SCD) is autosomal recessive disorder that is the result of a point mutation in the coding region of the beta globin gene. Polymerization of red blood cells with the sickle hemoglobin result in painful clinical symptoms and early death due to end organ failure. Improvement of treatment has extended the survival of adolescents into adulthood and offers relief of symptoms but does not offer a cure against the diagnosis being the inevitable cause of an early death. In addition, response to therapies vary between patients depending on their responsiveness and metabolism of medications. Hematopoietic stem cell transplantation offers reduction of recipient HgbS through replacing it with HgbA from the donor. Increased use of hematopoietic stem cell transplantation (HSCT) offers a curative therapy for patients with SCD that have access to an HLA-identical donor. However, limitations to indications for HSCT result due to associated toxicities with myeloablative conditioning and risk of graft failure. Reduced intensity and nonmyeloablative conditioning look at reducing associated toxicities and making HSCT readily available for the adult population through mixed chimerism. In addition, clinical trials looking at alternative donors and gene therapies expand the availability of HSCT for the vast majority of patients without an HLA-identical donor.

Keywords: sickle cell disease, stem cell, hemoglobinopathy, HSCT, allogeneic transplantation

Creative Commons Attribution License

©2020 McGill, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.