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Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic

BACKGROUND AND OBJECTIVES: Biological raw materials, the basis for cellular therapies such as stem cells, have a significantly greater degree of complexity than their traditional pharmaceutical counterparts. This can be attributed to the inherent variation of its source – human beings. Currently, ce...

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Autores principales: Thurman‐Newell, J. A., Petzing, J. N., Williams, D. J.
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/PMC5016773/
https://www.ncbi.nlm.nih.gov/pubmed/26174339
http://dx.doi.org/10.1111/vox.12288
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author Thurman‐Newell, J. A.
Petzing, J. N.
Williams, D. J.
author_facet Thurman‐Newell, J. A.
Petzing, J. N.
Williams, D. J.
author_sort Thurman‐Newell, J. A.
collection PubMed
description BACKGROUND AND OBJECTIVES: Biological raw materials, the basis for cellular therapies such as stem cells, have a significantly greater degree of complexity than their traditional pharmaceutical counterparts. This can be attributed to the inherent variation of its source – human beings. Currently, cell therapies are made in small, ad hoc batches, but larger scale production is a prerequisite to meeting future demand and will require a quality‐by‐design approach to manufacturing that will be designed around, or be robust to this variation. Quantification of variation will require understanding of the current baseline and stratification of its sources. MATERIALS AND METHODS: Haematopoietic stem cell therapy was chosen as a case study to explore this variation, and a PRISMA‐guided (Preferred Reporting Items for Systematic Reviews and Meta‐Analyses) systematic meta‐analysis was carried out for a number of predetermined cell measurements. RESULTS: From this data set, it appears that the extent of variation in therapeutic dose (in terms of transplanted total nucleated cells and CD34(+) cells per kilogram) for HSCT is between one and four orders of magnitude of the median. CONCLUSIONS: This is tolerated under the practice of medicine but would be unmanageable from a biomanufacturing perspective and raises concerns about comparable levels of efficacy and treatment. A number of sources that will contribute towards this variation are also reported, as is the direction of travel for 4 greater clarity of the scale of this challenge.
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spelling pubmed-50167732016-09-20 Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic Thurman‐Newell, J. A. Petzing, J. N. Williams, D. J. Vox Sang Cell Therapy BACKGROUND AND OBJECTIVES: Biological raw materials, the basis for cellular therapies such as stem cells, have a significantly greater degree of complexity than their traditional pharmaceutical counterparts. This can be attributed to the inherent variation of its source – human beings. Currently, cell therapies are made in small, ad hoc batches, but larger scale production is a prerequisite to meeting future demand and will require a quality‐by‐design approach to manufacturing that will be designed around, or be robust to this variation. Quantification of variation will require understanding of the current baseline and stratification of its sources. MATERIALS AND METHODS: Haematopoietic stem cell therapy was chosen as a case study to explore this variation, and a PRISMA‐guided (Preferred Reporting Items for Systematic Reviews and Meta‐Analyses) systematic meta‐analysis was carried out for a number of predetermined cell measurements. RESULTS: From this data set, it appears that the extent of variation in therapeutic dose (in terms of transplanted total nucleated cells and CD34(+) cells per kilogram) for HSCT is between one and four orders of magnitude of the median. CONCLUSIONS: This is tolerated under the practice of medicine but would be unmanageable from a biomanufacturing perspective and raises concerns about comparable levels of efficacy and treatment. A number of sources that will contribute towards this variation are also reported, as is the direction of travel for 4 greater clarity of the scale of this challenge. John Wiley and Sons Inc. 2015-07-14 2015-11 /pmc/articles/PMC5016773/ /pubmed/26174339 http://dx.doi.org/10.1111/vox.12288 Text en © 2015 The Authors. Vox Sanguinis published by John Wiley & Sons Ltd on behalf of International Society of Blood Transfusion This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cell Therapy
Thurman‐Newell, J. A.
Petzing, J. N.
Williams, D. J.
Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title_full Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title_fullStr Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title_full_unstemmed Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title_short Quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
title_sort quantification of biological variation in blood‐based therapy – a summary of a meta‐analysis to inform manufacturing in the clinic
topic Cell Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016773/
https://www.ncbi.nlm.nih.gov/pubmed/26174339
http://dx.doi.org/10.1111/vox.12288
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