Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8648152 | Blood Cells, Molecules, and Diseases | 2017 | 34 Pages |
Abstract
Despite sickle cell disease (SCD) first being reported >Â 100Â years ago and molecularly characterized >Â 50Â years ago, patients continue to experience severe morbidity and early mortality. Although there have been substantial clinical advances with immunizations, penicillin prophylaxis, hydroxyurea treatment, and transfusion therapy, the only cure that can be offered is hematopoietic stem cell transplantation (HSCT). In this work, we summarize the various allogeneic curative approaches reported to date and discuss open and upcoming clinical research protocols. Then we consider gene therapy and gene editing strategies that may enable cure based on autologous HSCs.
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Authors
Daniel E. Bauer, Christian Brendel, Courtney D. Fitzhugh,