Stem Cells To Cure Sickle Cell Anemia

Authors

  • Tolulope O. Rosanwo Division of Pediatric Hematology/Oncology, Boston Children's Hospital and Dana Farber Cancer Institute, Boston, MA, USA; Stem Cell Transplantation Program, Boston Children's Hospital; Case Western Reserve University School of Medicine, Cleveland, OH, USA Author

DOI:

https://doi.org/10.65539/056mjw33

Keywords:

sickle cell anemia, stem cell transplantation, HSCT, gene therapy, genome editing

Abstract

Sickle cell anemia (SCA) is one of the most prevalent genetic disorders in the world and the most common congenital anemia in the United States. The severity of SCA spans from mild clinical cases, managed by careful living, to severe cases involving bone crises, infection, stroke, and multi-organ failure. Hematopoietic stem cell transplantation (HSCT) is the most widely known and effective method to cure the disease and is used today in only severe cases due to risks of graft rejection and fatal infections. The use of stem cells for the cure of sickle cell disease from the early days of transplantation to the most recent breakthroughs in stem cell therapy, gene therapy and genome-editing will be examined in this review.

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Published

2020-02-28

How to Cite

Stem Cells To Cure Sickle Cell Anemia. (2020). Harvard Medical Student Review, 5(1), 27-31. https://doi.org/10.65539/056mjw33

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