- New
- Research Article
- 10.1016/s1079-9796(25)00065-8
- Feb 1, 2026
- Blood Cells, Molecules, and Diseases
- Research Article
- 10.1016/s1079-9796(25)00037-3
- Jul 1, 2025
- Blood Cells, Molecules, and Diseases
- Research Article
- 10.1016/j.bcmd.2025.102934
- Jul 1, 2025
- Blood Cells, Molecules, and Diseases
- Guzmán López De Hontanar Torres + 7 more
- Research Article
- 10.1016/s1079-9796(25)00020-8
- May 1, 2025
- Blood Cells, Molecules, and Diseases
- Research Article
- 10.1016/s1079-9796(25)00008-7
- Mar 1, 2025
- Blood Cells, Molecules, and Diseases
- Front Matter
- 10.1016/s1079-9796(24)00024-x
- May 1, 2024
- Blood Cells, Molecules, and Diseases
- Front Matter
- 10.1016/s1079-9796(24)00011-1
- Feb 2, 2024
- Blood Cells, Molecules, and Diseases
- Research Article
4
- 10.1016/j.bcmd.2024.102828
- Jan 20, 2024
- Blood Cells, Molecules, and Diseases
- Paul Boma Muteb + 9 more
- Research Article
3
- 10.1016/j.bcmd.2024.102824
- Jan 19, 2024
- Blood Cells, Molecules, and Diseases
- Avital Mendelson + 3 more
In preparation for hematopoietic stem cell mobilization and collection, current ex vivo gene therapy protocols for sickle cell disease require patients to undergo several months of chronic red cell transfusion. For health care equity, alternatives to red cell transfusion should be available. We examined whether treatment with GBT1118, the murine analog of voxelotor, could be a safe and feasible alternative to red cell transfusion. We found that 3 weeks of treatment with GBT1118 increased the percentage of bone marrow hematopoietic stem cells and upon plerixafor mobilization, the percentage of peripheral blood hematopoietic stem cells. Our data suggest that voxelotor should be further explored for its potential safety and utility as preparation for hematopoietic stem cell mobilization and collection.
- Discussion
- 10.1016/j.bcmd.2024.102826
- Jan 17, 2024
- Blood Cells, Molecules, and Diseases
- Sangsang Wang + 2 more