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Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations
BACKGROUND AND OBJECTIVES: Plasma pools for the production of human plasma medicinal products are distinguished according to the collection method (recovered or apheresis plasma) and the donor remuneration status. National regulations and the physical status of the donor determine the donation frequ...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001115/ https://www.ncbi.nlm.nih.gov/pubmed/20840337 http://dx.doi.org/10.1111/j.1423-0410.2010.01345.x |
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author | Laub, R Baurin, S Timmerman, D Branckaert, T Strengers, P |
author_facet | Laub, R Baurin, S Timmerman, D Branckaert, T Strengers, P |
author_sort | Laub, R |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Plasma pools for the production of human plasma medicinal products are distinguished according to the collection method (recovered or apheresis plasma) and the donor remuneration status. National regulations and the physical status of the donor determine the donation frequency and plasma volume per session. Relevant protein contents of different types of pools have not fully been compared. MATERIALS AND METHODS: We compared the levels of total protein, 15 main relevant plasma protein markers, and anti-B19 and anti-Streptococcus pneumoniae IgG in single-type pools of donations from different countries (Belgium, Finland, France, the Netherlands, Germany, United States). Both recovered plasma from non-remunerated donors and apheresis plasma from remunerated and non-remunerated donors were studied. RESULTS: Pools from paid US high-frequency, high-volume plasmapheresis donors showed significantly lower total protein (−9%), albumin (−15%), total IgG (−24%), IgM (−28%), hemopexin (−11%) and retinol-binding protein (−10%) but higher C1-inhibitor, pre-albumin and C-reactive protein contents than pools from unpaid European Union (EU) or US whole-blood or plasmapheresis donors. In contrast to pools from compensated EU plasmapheresis donors, pools from unpaid whole-blood or plasmapheresis donors showed no significant differences, whatever the collection method or country. Reductions in specific protein contents correlated well with protein half-life. CONCLUSION: These results should be taken into account with regard to donor health management and protein recovery. |
format | Text |
id | pubmed-3001115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-30011152010-12-31 Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations Laub, R Baurin, S Timmerman, D Branckaert, T Strengers, P Vox Sang Blood-Component Collection and Production BACKGROUND AND OBJECTIVES: Plasma pools for the production of human plasma medicinal products are distinguished according to the collection method (recovered or apheresis plasma) and the donor remuneration status. National regulations and the physical status of the donor determine the donation frequency and plasma volume per session. Relevant protein contents of different types of pools have not fully been compared. MATERIALS AND METHODS: We compared the levels of total protein, 15 main relevant plasma protein markers, and anti-B19 and anti-Streptococcus pneumoniae IgG in single-type pools of donations from different countries (Belgium, Finland, France, the Netherlands, Germany, United States). Both recovered plasma from non-remunerated donors and apheresis plasma from remunerated and non-remunerated donors were studied. RESULTS: Pools from paid US high-frequency, high-volume plasmapheresis donors showed significantly lower total protein (−9%), albumin (−15%), total IgG (−24%), IgM (−28%), hemopexin (−11%) and retinol-binding protein (−10%) but higher C1-inhibitor, pre-albumin and C-reactive protein contents than pools from unpaid European Union (EU) or US whole-blood or plasmapheresis donors. In contrast to pools from compensated EU plasmapheresis donors, pools from unpaid whole-blood or plasmapheresis donors showed no significant differences, whatever the collection method or country. Reductions in specific protein contents correlated well with protein half-life. CONCLUSION: These results should be taken into account with regard to donor health management and protein recovery. Blackwell Publishing Ltd 2010-10 /pmc/articles/PMC3001115/ /pubmed/20840337 http://dx.doi.org/10.1111/j.1423-0410.2010.01345.x Text en Copyright Vox Sanguinis © 2010 International Society of Blood Transfusion http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Blood-Component Collection and Production Laub, R Baurin, S Timmerman, D Branckaert, T Strengers, P Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title | Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title_full | Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title_fullStr | Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title_full_unstemmed | Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title_short | Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
title_sort | specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations |
topic | Blood-Component Collection and Production |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001115/ https://www.ncbi.nlm.nih.gov/pubmed/20840337 http://dx.doi.org/10.1111/j.1423-0410.2010.01345.x |
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