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Cord blood processing by a novel filtration system

OBJECTIVES: Availability of cord blood (CB) processing has been limited by the need for electrically aided centrifugal techniques, which often produce only low final cell product yield. Here, we describe development and characterization of a novel filter device aimed at allowing CB processing, using...

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Detalles Bibliográficos
Autores principales: Sato, N., Fricke, C., McGuckin, C., Forraz, N., Degoul, O., Atzeni, G., Sakurai, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496033/
https://www.ncbi.nlm.nih.gov/pubmed/26456086
http://dx.doi.org/10.1111/cpr.12217
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author Sato, N.
Fricke, C.
McGuckin, C.
Forraz, N.
Degoul, O.
Atzeni, G.
Sakurai, H.
author_facet Sato, N.
Fricke, C.
McGuckin, C.
Forraz, N.
Degoul, O.
Atzeni, G.
Sakurai, H.
author_sort Sato, N.
collection PubMed
description OBJECTIVES: Availability of cord blood (CB) processing has been limited by the need for electrically aided centrifugal techniques, which often produce only low final cell product yield. Here, we describe development and characterization of a novel filter device aimed at allowing CB processing, using gentle gravity‐led flow. MATERIALS AND METHODS: CB was processed with a novel filter device (CellEffic CB, consisting of non‐woven fabric), without any centrifugation. Cells were harvested by flushing the filter with either HES or physiological saline solution (SALINE). Differential cell counts and viability analysis, combined with Fluorescence‐Activated Cell Sorting (FACS) (total nucleated cells [TNC], mononuclear cells [MNC], CD45+ CD34+ cells, hematopoietic precursor cells [HPCs]) and clonogenic assay, were employed for analysis of CB pre‐ and post‐processing, and after freeze/thawing. RESULTS: Processing using the novel filter yielded high quality RBC depletion while maintaining good recovery of TNC, MNC, CD34+, HPCs and colony forming unit (CFU) output. The filter performed equally well using HES or SALINE. Gravity‐led flow provided gentle cell movement and protection of the stem cell compartment. Post‐thaw CFU output was maintained particularly, an important indicator for CB banking. CONCLUSIONS: Geographical limitations of CB transplantation and banking have required a non‐electrical, non‐centrifugal solution. This novel filter CellEffic CB device revealed rapid yet gentle cell processing while maintaining the stem/progenitor cell compartment required for both haematological and regenerative medicine therapies.
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spelling pubmed-64960332020-03-13 Cord blood processing by a novel filtration system Sato, N. Fricke, C. McGuckin, C. Forraz, N. Degoul, O. Atzeni, G. Sakurai, H. Cell Prolif Original Articles OBJECTIVES: Availability of cord blood (CB) processing has been limited by the need for electrically aided centrifugal techniques, which often produce only low final cell product yield. Here, we describe development and characterization of a novel filter device aimed at allowing CB processing, using gentle gravity‐led flow. MATERIALS AND METHODS: CB was processed with a novel filter device (CellEffic CB, consisting of non‐woven fabric), without any centrifugation. Cells were harvested by flushing the filter with either HES or physiological saline solution (SALINE). Differential cell counts and viability analysis, combined with Fluorescence‐Activated Cell Sorting (FACS) (total nucleated cells [TNC], mononuclear cells [MNC], CD45+ CD34+ cells, hematopoietic precursor cells [HPCs]) and clonogenic assay, were employed for analysis of CB pre‐ and post‐processing, and after freeze/thawing. RESULTS: Processing using the novel filter yielded high quality RBC depletion while maintaining good recovery of TNC, MNC, CD34+, HPCs and colony forming unit (CFU) output. The filter performed equally well using HES or SALINE. Gravity‐led flow provided gentle cell movement and protection of the stem cell compartment. Post‐thaw CFU output was maintained particularly, an important indicator for CB banking. CONCLUSIONS: Geographical limitations of CB transplantation and banking have required a non‐electrical, non‐centrifugal solution. This novel filter CellEffic CB device revealed rapid yet gentle cell processing while maintaining the stem/progenitor cell compartment required for both haematological and regenerative medicine therapies. John Wiley and Sons Inc. 2015-10-12 /pmc/articles/PMC6496033/ /pubmed/26456086 http://dx.doi.org/10.1111/cpr.12217 Text en © 2015 Kaneka Corporation. Cell Proliferation Published John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Sato, N.
Fricke, C.
McGuckin, C.
Forraz, N.
Degoul, O.
Atzeni, G.
Sakurai, H.
Cord blood processing by a novel filtration system
title Cord blood processing by a novel filtration system
title_full Cord blood processing by a novel filtration system
title_fullStr Cord blood processing by a novel filtration system
title_full_unstemmed Cord blood processing by a novel filtration system
title_short Cord blood processing by a novel filtration system
title_sort cord blood processing by a novel filtration system
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496033/
https://www.ncbi.nlm.nih.gov/pubmed/26456086
http://dx.doi.org/10.1111/cpr.12217
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