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Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities

BACKGROUND: Therapeutic allogeneic mesenchymal stromal cells (MSCs) are currently in clinical trials to evaluate their effectiveness in treating many different disease indications. Eventual commercialization for broad distribution will require further improvements in manufacturing processes to econo...

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Autores principales: Johnstone, Brian H., Miller, Hannah M., Beck, Madelyn R., Gu, Dongsheng, Thirumala, Sreedhar, LaFontaine, Michael, Brandacher, Gerald, Woods, Erik J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919862/
https://www.ncbi.nlm.nih.gov/pubmed/32873509
http://dx.doi.org/10.1016/j.jcyt.2020.07.003
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author Johnstone, Brian H.
Miller, Hannah M.
Beck, Madelyn R.
Gu, Dongsheng
Thirumala, Sreedhar
LaFontaine, Michael
Brandacher, Gerald
Woods, Erik J.
author_facet Johnstone, Brian H.
Miller, Hannah M.
Beck, Madelyn R.
Gu, Dongsheng
Thirumala, Sreedhar
LaFontaine, Michael
Brandacher, Gerald
Woods, Erik J.
author_sort Johnstone, Brian H.
collection PubMed
description BACKGROUND: Therapeutic allogeneic mesenchymal stromal cells (MSCs) are currently in clinical trials to evaluate their effectiveness in treating many different disease indications. Eventual commercialization for broad distribution will require further improvements in manufacturing processes to economically manufacture MSCs at scales sufficient to satisfy projected demands. A key contributor to the present high cost of goods sold for MSC manufacturing is the need to create master cell banks from multiple donors, which leads to variability in large-scale manufacturing runs. Therefore, the availability of large single donor depots of primary MSCs would greatly benefit the cell therapy market by reducing costs associated with manufacturing. METHODS: We have discovered that an abundant population of cells possessing all the hallmarks of MSCs is tightly associated with the vertebral body (VB) bone matrix and only liberated by proteolytic digestion. Here we demonstrate that these vertebral bone-adherent (vBA) MSCs possess all the International Society of Cell and Gene Therapy-defined characteristics (e.g., plastic adherence, surface marker expression and trilineage differentiation) of MSCs, and we have therefore termed them vBA-MSCs to distinguish this population from loosely associated MSCs recovered through aspiration or rinsing of the bone marrow compartment. RESULTS: Pilot banking and expansion were performed with vBA-MSCs obtained from 3 deceased donors, and it was demonstrated that bank sizes averaging 2.9 × 10(8) ± 1.35 × 10(8) vBA-MSCs at passage 1 were obtainable from only 5 g of digested VB bone fragments. Each bank of cells demonstrated robust proliferation through a total of 9 passages, without significant reduction in population doubling times. The theoretical total cell yield from the entire amount of bone fragments (approximately 300 g) from each donor with limited expansion through 4 passages is 100 trillion (1 × 10(14)) vBA-MSCs, equating to over 10(5) doses at 10 × 10(6) cells/kg for an average 70-kg recipient. DISCUSSION: Thus, we have established a novel and plentiful source of MSCs that will benefit the cell therapy market by overcoming manufacturing and regulatory inefficiencies due to donor-to-donor variability.
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spelling pubmed-89198622022-03-14 Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities Johnstone, Brian H. Miller, Hannah M. Beck, Madelyn R. Gu, Dongsheng Thirumala, Sreedhar LaFontaine, Michael Brandacher, Gerald Woods, Erik J. Cytotherapy Article BACKGROUND: Therapeutic allogeneic mesenchymal stromal cells (MSCs) are currently in clinical trials to evaluate their effectiveness in treating many different disease indications. Eventual commercialization for broad distribution will require further improvements in manufacturing processes to economically manufacture MSCs at scales sufficient to satisfy projected demands. A key contributor to the present high cost of goods sold for MSC manufacturing is the need to create master cell banks from multiple donors, which leads to variability in large-scale manufacturing runs. Therefore, the availability of large single donor depots of primary MSCs would greatly benefit the cell therapy market by reducing costs associated with manufacturing. METHODS: We have discovered that an abundant population of cells possessing all the hallmarks of MSCs is tightly associated with the vertebral body (VB) bone matrix and only liberated by proteolytic digestion. Here we demonstrate that these vertebral bone-adherent (vBA) MSCs possess all the International Society of Cell and Gene Therapy-defined characteristics (e.g., plastic adherence, surface marker expression and trilineage differentiation) of MSCs, and we have therefore termed them vBA-MSCs to distinguish this population from loosely associated MSCs recovered through aspiration or rinsing of the bone marrow compartment. RESULTS: Pilot banking and expansion were performed with vBA-MSCs obtained from 3 deceased donors, and it was demonstrated that bank sizes averaging 2.9 × 10(8) ± 1.35 × 10(8) vBA-MSCs at passage 1 were obtainable from only 5 g of digested VB bone fragments. Each bank of cells demonstrated robust proliferation through a total of 9 passages, without significant reduction in population doubling times. The theoretical total cell yield from the entire amount of bone fragments (approximately 300 g) from each donor with limited expansion through 4 passages is 100 trillion (1 × 10(14)) vBA-MSCs, equating to over 10(5) doses at 10 × 10(6) cells/kg for an average 70-kg recipient. DISCUSSION: Thus, we have established a novel and plentiful source of MSCs that will benefit the cell therapy market by overcoming manufacturing and regulatory inefficiencies due to donor-to-donor variability. 2020-11 2020-08-30 /pmc/articles/PMC8919862/ /pubmed/32873509 http://dx.doi.org/10.1016/j.jcyt.2020.07.003 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Johnstone, Brian H.
Miller, Hannah M.
Beck, Madelyn R.
Gu, Dongsheng
Thirumala, Sreedhar
LaFontaine, Michael
Brandacher, Gerald
Woods, Erik J.
Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title_full Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title_fullStr Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title_full_unstemmed Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title_short Identification and Characterization of a large Source of Primary mesenchymal stem cells tightly adhered to bone Surfaces of human vertebral body marrow cavities
title_sort identification and characterization of a large source of primary mesenchymal stem cells tightly adhered to bone surfaces of human vertebral body marrow cavities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919862/
https://www.ncbi.nlm.nih.gov/pubmed/32873509
http://dx.doi.org/10.1016/j.jcyt.2020.07.003
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