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Systematic investigation of oxygen and growth factors in clinically valid ex vivo expansion of cord blood CD34+ hematopoietic progenitor cells
journal contribution
posted on 2012-07-01, 00:00 authored by M Tursky, Fiona Collier, Alister WardAlister Ward, M KirklandBackground aims. Cord blood is considered to be a superior source of hematopoietic stem and progenitor cells for transplantation, but clinical use is limited primarily because of the low numbers of cells harvested. Ex vivo expansion has the potential to provide a safe, effective means of increasing cell numbers. However, an absence of consensus regarding optimum expansion conditions prevents standard implementation. Many studies lack clinical applicability, or have failed to investigate the combinational effects of different parameters.
Methods. This is the first study to characterize systematically the effect of growth factor combinations across multiple oxygen levels on the ex vivo expansion of cord blood CD34 hematopoietic cells utilizing clinically approvable reagents and methodologies throughout.
Results. Optimal fold expansion, as assessed both phenotypically and functionally, was greatest with thrombopoietin, stem cell factor, Flt-3 ligand and interleukin-6 at an oxygen level of 10%. With these conditions, serial expansion showed continual target population expansion and consistently higher expression levels of self-renewal associated genes.
Conclusions. This study has identified optimized fold expansion conditions, with the potential for direct clinical translation to increase transplantable cell dose and as a baseline methodology against which future factors can be tested.
Methods. This is the first study to characterize systematically the effect of growth factor combinations across multiple oxygen levels on the ex vivo expansion of cord blood CD34 hematopoietic cells utilizing clinically approvable reagents and methodologies throughout.
Results. Optimal fold expansion, as assessed both phenotypically and functionally, was greatest with thrombopoietin, stem cell factor, Flt-3 ligand and interleukin-6 at an oxygen level of 10%. With these conditions, serial expansion showed continual target population expansion and consistently higher expression levels of self-renewal associated genes.
Conclusions. This study has identified optimized fold expansion conditions, with the potential for direct clinical translation to increase transplantable cell dose and as a baseline methodology against which future factors can be tested.
History
Journal
CytotherapyVolume
14Issue
6Pagination
679 - 685Publisher
ElsevierLocation
Oxford, EnglandPublisher DOI
ISSN
1465-3249eISSN
1477-2566Language
engPublication classification
C1 Refereed article in a scholarly journalUsage metrics
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Categories
Keywords
cord bloodex vivo expansiongrowth factorshematopoiesishematopoietic progenitor cellsoxygenstem cell transplantationScience & TechnologyLife Sciences & BiomedicineCell & Tissue EngineeringBiotechnology & Applied MicrobiologyCell BiologyHematologyMedicine, Research & ExperimentalResearch & Experimental MedicineSCID-REPOPULATING CELLSBONE-MARROW CELLSSTEM-CELLSSELF-RENEWALINTERLEUKIN-6 IL-6C-KITTRANSPLANTATIONMAINTENANCENICHESRECONSTITUTION