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Redirection of transfusion waste and by-products for xeno-free research applications
BACKGROUND AND AIM: Whole blood is processed to derive a red cell concentrate, plasma, and buffy coat (BC) (from which platelets can be further extracted). Unused plasma and BCs are common in most blood establishments and considered a liability. The redirection of these products to xeno-free applica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Whioce Publishing Pte. Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7197051/ https://www.ncbi.nlm.nih.gov/pubmed/32377579 |
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author | Zammit, Vanessa Farrugia, Mark Baron, Byron |
author_facet | Zammit, Vanessa Farrugia, Mark Baron, Byron |
author_sort | Zammit, Vanessa |
collection | PubMed |
description | BACKGROUND AND AIM: Whole blood is processed to derive a red cell concentrate, plasma, and buffy coat (BC) (from which platelets can be further extracted). Unused plasma and BCs are common in most blood establishments and considered a liability. The redirection of these products to xeno-free applications is not complicated or time-consuming and cannot only benefit the research recipients but also the blood establishment suppliers interested in research collaboration. The aim of this study is to describe a diverse yet by no means an exhaustive list of options for preparing blood products for research applications. MATERIALS AND METHODS: Plasma and BCs from healthy donors were processed using basic laboratory techniques under aseptic conditions and tested for their ability to support the culture of mesenchymal stem cells in both 2D and 3D cultures using fibrin clots. The white blood cells (WBC) from the BCs were induced by phytohemagglutinin and CD marker expression was monitored using quantitative polymerase chain reaction. RESULTS: All the methods tested for preparing blood products were successful but the applicability to different settings varied greatly with the most successful being the supplementation of Dulbecco’s Modified Eagle Medium: Nutrient Mixture F-12 with 20% cryodepleted plasma and 0.1 mg/mL platelet lysate, the formation of fibrin clots using a ratio of 3:1 (medium: plasma) and the culturing of WBCs with 5 µg/mL phytohemagglutinin. CONCLUSIONS: Using the wastes and by-products of blood establishments for xeno-free cell culturing of stem cells will reduce the reliance on commercially available, ready-made products, and increasing the potential for therapeutic stem cell research. Despite the benefits presented both in terms of cost and applications, further characterization and optimization of each blood product for reproducibility of results is required. RELEVANCE FOR PATIENTS: The availability of low-cost xeno-free reagents will speed up therapeutic stem cell research and allow patients to receive treatments of the expected high standards at lower costs. |
format | Online Article Text |
id | pubmed-7197051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Whioce Publishing Pte. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71970512020-05-06 Redirection of transfusion waste and by-products for xeno-free research applications Zammit, Vanessa Farrugia, Mark Baron, Byron J Clin Transl Res Review Article BACKGROUND AND AIM: Whole blood is processed to derive a red cell concentrate, plasma, and buffy coat (BC) (from which platelets can be further extracted). Unused plasma and BCs are common in most blood establishments and considered a liability. The redirection of these products to xeno-free applications is not complicated or time-consuming and cannot only benefit the research recipients but also the blood establishment suppliers interested in research collaboration. The aim of this study is to describe a diverse yet by no means an exhaustive list of options for preparing blood products for research applications. MATERIALS AND METHODS: Plasma and BCs from healthy donors were processed using basic laboratory techniques under aseptic conditions and tested for their ability to support the culture of mesenchymal stem cells in both 2D and 3D cultures using fibrin clots. The white blood cells (WBC) from the BCs were induced by phytohemagglutinin and CD marker expression was monitored using quantitative polymerase chain reaction. RESULTS: All the methods tested for preparing blood products were successful but the applicability to different settings varied greatly with the most successful being the supplementation of Dulbecco’s Modified Eagle Medium: Nutrient Mixture F-12 with 20% cryodepleted plasma and 0.1 mg/mL platelet lysate, the formation of fibrin clots using a ratio of 3:1 (medium: plasma) and the culturing of WBCs with 5 µg/mL phytohemagglutinin. CONCLUSIONS: Using the wastes and by-products of blood establishments for xeno-free cell culturing of stem cells will reduce the reliance on commercially available, ready-made products, and increasing the potential for therapeutic stem cell research. Despite the benefits presented both in terms of cost and applications, further characterization and optimization of each blood product for reproducibility of results is required. RELEVANCE FOR PATIENTS: The availability of low-cost xeno-free reagents will speed up therapeutic stem cell research and allow patients to receive treatments of the expected high standards at lower costs. Whioce Publishing Pte. Ltd. 2019-11-09 /pmc/articles/PMC7197051/ /pubmed/32377579 Text en Copyright © 2019, Whioce Publishing Pte. Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This work is licensed under a Creative Commons Attribution 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Review Article Zammit, Vanessa Farrugia, Mark Baron, Byron Redirection of transfusion waste and by-products for xeno-free research applications |
title | Redirection of transfusion waste and by-products for xeno-free research applications |
title_full | Redirection of transfusion waste and by-products for xeno-free research applications |
title_fullStr | Redirection of transfusion waste and by-products for xeno-free research applications |
title_full_unstemmed | Redirection of transfusion waste and by-products for xeno-free research applications |
title_short | Redirection of transfusion waste and by-products for xeno-free research applications |
title_sort | redirection of transfusion waste and by-products for xeno-free research applications |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7197051/ https://www.ncbi.nlm.nih.gov/pubmed/32377579 |
work_keys_str_mv | AT zammitvanessa redirectionoftransfusionwasteandbyproductsforxenofreeresearchapplications AT farrugiamark redirectionoftransfusionwasteandbyproductsforxenofreeresearchapplications AT baronbyron redirectionoftransfusionwasteandbyproductsforxenofreeresearchapplications |