| Autor: |
Tolu SS; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Wang K; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Yan Z; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Zhang S; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Roberts K; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Crouch AS; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Sebastian G; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Chaitowitz M; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Fornari ED; Department of Orthopedic Surgery, Montefiore Medical Center, Bronx, NY 10461, USA., Schwechter EM; Department of Orthopedic Surgery, Montefiore Medical Center, Bronx, NY 10461, USA., Uehlinger J; Department of Pathology, Division of Transfusion Medicine, Montefiore Health System, Bronx, NY 10467, USA., Manwani D; Pediatric Hematology/Oncology/Marrow and Blood Cell Transplantation, Montefiore Health System, Bronx, NY 10467, USA., Minniti CP; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA., Bouhassira EE; Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA. |
| Abstrakt: |
The consequences of sickle cell disease (SCD) include ongoing hematopoietic stress, hemolysis, vascular damage, and effect of chronic therapies, such as blood transfusions and hydroxyurea, on hematopoietic stem and progenitor cell (HSPC) have been poorly characterized. We have quantified the frequencies of nine HSPC populations by flow cytometry in the peripheral blood of pediatric and adult patients, stratified by treatment and control cohorts. We observed broad differences between SCD patients and healthy controls. SCD is associated with 10 to 20-fold increase in CD34 dim cells, a two to five-fold increase in CD34 bright cells, a depletion in Megakaryocyte-Erythroid Progenitors, and an increase in hematopoietic stem cells, when compared to controls. SCD is also associated with abnormal expression of CD235a as well as high levels CD49f antigen expression. These findings were present to varying degrees in all patients with SCD, including those on chronic therapy and those who were therapy naive. HU treatment appeared to normalize many of these parameters. Chronic stress erythropoiesis and inflammation incited by SCD and HU therapy have long been suspected of causing premature aging of the hematopoietic system, and potentially increasing the risk of hematological malignancies. An important finding of this study was that the observed concentration of CD34 bright cells and of all the HSPCs decreased logarithmically with time of treatment with HU. This correlation was independent of age and specific to HU treatment. Although the number of circulating HSPCs is influenced by many parameters, our findings suggest that HU treatment may decrease premature aging and hematologic malignancy risk compared to the other therapeutic modalities in SCD. |
