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Megakaryocyte Heterogeneity in Sickle Cell Disease
Sponsor: Centre Hospitalier Universitaire de la Guadeloupe
Summary
Sickle cell disease (SCD) is characterized by chronic hemolytic anemia, painful crisis called vaso-occlusive crisis (VOC) and chronic inflammation. Activated platelets of SCD patients participated to both chronic inflammation and painful VOC. Platelets are anucleated cells from the fragmentation of megakaryocytes in bone marrow. The main aim of this study is to characterize the distribution of the different megakaryocyte subpopulations of sickle cell disease patients SS and SC and in particular the "immune" megakaryocytes CD148+CD48+ and to compare it with the platelet phenotype.
Official title: Characterization of Megakaryocytic Subpopulations and the "Immune" Phenotype of Platelets of the Sickle Cell Disease Patient
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2025-07
Completion Date
2027-03
Last Updated
2025-05-25
Healthy Volunteers
Yes
Conditions
Locations (1)
Chu de La Guadeloupe
Pointe-à-Pitre, Guadeloupe