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Ischemia considerations for the development of an organ and tissue donor derived bone marrow bank
- Source :
- Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020), Journal of Translational Medicine
- Publication Year :
- 2020
- Publisher :
- Research Square Platform LLC, 2020.
-
Abstract
- Background Deceased organ donors represent an untapped source of therapeutic bone marrow (BM) that can be recovered in 3–5 times the volume of that obtained from living donors, tested for quality, cryopreserved, and banked indefinitely for future on-demand use. A challenge for a future BM banking system will be to manage the prolonged ischemia times that are inevitable when bones procured at geographically-dispersed locations are shipped to distant facilities for processing. Our objectives were to: (a) quantify, under realistic field conditions, the relationship between ischemia time and the quality of hematopoietic stem and progenitor cells (HSPCs) derived from deceased-donor BM; (b) identify ischemia-time boundaries beyond which HSPC quality is adversely affected; (c) investigate whole-body cooling as a strategy for preserving cell quality; and (d) investigate processing experience as a variable affecting quality. Methods Seventy-five bones from 62 donors were analyzed for CD34+ viability following their exposure to various periods of warm-ischemia time (WIT), cold-ischemia time (CIT), and body-cooling time (BCT). Regression models were developed to quantify the independent associations of WIT, CIT, and BCT, with the viability and function of recovered HSPCs. Results Results demonstrate that under “real-world” scenarios: (a) combinations of warm- and cold-ischemia times favorable to the recovery of high-quality HSPCs are achievable (e.g., CD34+ cell viabilities in the range of 80–90% were commonly observed); (b) body cooling prior to bone recovery is detrimental to cell viability (e.g., CD34+ viability with, vs. > 89% without body cooling); (c) vertebral bodies (VBs) are a superior source of HSPCs compared to ilia (IL) (e.g., %CD34+ viability > 80% when VBs were the source, vs. Conclusions Our models can be used by an emerging BM banking system to formulate ischemia-time tolerance limits and data-driven HSPC quality-acceptance standards.
- Subjects :
- 0301 basic medicine
Donor tissue
Ischemia
CD34
lcsh:Medicine
Antigens, CD34
Bone Marrow Cells
General Biochemistry, Genetics and Molecular Biology
Cryopreservation
Andrology
Bone marrow ischemia time
03 medical and health sciences
0302 clinical medicine
Bone Marrow
Bone marrow banking
Medicine
Humans
Deceased-donor bone marrow
Viability assay
Progenitor cell
Bone Marrow Transplantation
business.industry
Research
lcsh:R
General Medicine
medicine.disease
Hematopoietic Stem Cells
Tissue Donors
Haematopoiesis
030104 developmental biology
medicine.anatomical_structure
030220 oncology & carcinogenesis
Bone marrow
Hematopoietic stem cell transplant
business
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020), Journal of Translational Medicine
- Accession number :
- edsair.doi.dedup.....662dfc762eead5ce1cd45a915efbdf11
- Full Text :
- https://doi.org/10.21203/rs.3.rs-24976/v2