Abstract
Sickle cell disease (SCD) is a severe genetic blood disorder characterized by hemolytic anemia, episodic vaso-occlusion, and progressive organ damage. Current management of the disease remains symptomatic or preventative. Specific treatment targeting major complications such as vasoocclusion is still lacking. Recent studies have identified various cellular and molecular factors that contribute to the pathophysiology of SCD. Here, we review the role of these elements and discuss the opportunities for therapeutic intervention.
Original language | English (US) |
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Pages (from-to) | 801-809 |
Number of pages | 9 |
Journal | Blood |
Volume | 127 |
Issue number | 7 |
DOIs | |
State | Published - Feb 18 2016 |
ASJC Scopus subject areas
- Biochemistry
- Immunology
- Hematology
- Cell Biology