Abstract
Cryopreservation is often used as a means of storing haematopoietic progenitor cell-apheresis (HPC-A) product when it is collected as part of high-dose therapy for the treatment of haematological malignancies. Processing and cryopreservation of HPC-A is known to reduce the viability and the absolute number of CD34+ cells available for reinfusion.1,2 Therefore, a pilot vial (PV) containing a small aliquot of the same HPC-A material is usually cryopreserved and stored under the same conditions enabling enumeration and viability assessment on post-thaw HPC-A material without disturbing the primary infusion bag required for the transplantation. However, whether PV material can be used to assess other functional or phenotypic stem cell markers in HPC-A material following cryopreservation has not been fully investigated. We aimed to assess whether markers of viability, early apoptosis, DNA damage signalling and oxidative damage, together with CD34+ subset analysis performed similarly between PV and HPC-A material following cryopreservation
| Original language | English |
|---|---|
| Pages (from-to) | 1631-1632 |
| Number of pages | 2 |
| Journal | Bone Marrow Transplantation |
| Volume | 51 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 1 Dec 2016 |
| Externally published | Yes |
Keywords
- Apoptosis Cell Survival Cryopreservation
- methods DNA Damage Hematopoietic Stem Cells
- cytology Hodgkin Disease
- blood/therapy Humans Linear Models Lymphoma, Non-Hodgkin
- blood
- therapy Membrane Potentials Multiple Myeloma
- therapy Oxygen
- chemistry Phenotype Pilot Projects Reactive Oxygen Species
- metabolism Signal Transduction Stem Cells
- cytology
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