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Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation

Neutropenia is a common side-effect of acute myeloid leukemia (AML) chemotherapy characterized by a critical drop in neutrophil blood concentration. Neutropenic patients are prone to infections, experience poorer clinical outcomes, and require expensive medical care. Although transfusions of donor n...

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Autores principales: Torres-Acosta, Mario A., Harrison, Richard P., Csaszar, Elizabeth, Rito-Palomares, Marco, Brunck, Marion E. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405517/
https://www.ncbi.nlm.nih.gov/pubmed/30881955
http://dx.doi.org/10.3389/fmed.2019.00021
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author Torres-Acosta, Mario A.
Harrison, Richard P.
Csaszar, Elizabeth
Rito-Palomares, Marco
Brunck, Marion E. G.
author_facet Torres-Acosta, Mario A.
Harrison, Richard P.
Csaszar, Elizabeth
Rito-Palomares, Marco
Brunck, Marion E. G.
author_sort Torres-Acosta, Mario A.
collection PubMed
description Neutropenia is a common side-effect of acute myeloid leukemia (AML) chemotherapy characterized by a critical drop in neutrophil blood concentration. Neutropenic patients are prone to infections, experience poorer clinical outcomes, and require expensive medical care. Although transfusions of donor neutrophils are a logical solution to neutropenia, this approach has not gained clinical traction, primarily due to challenges associated with obtaining sufficiently large numbers of neutrophils from donors whilst logistically managing their extremely short shelf-life. A protocol has been developed that produces clinical-scale quantities of neutrophils from hematopoietic stem and progenitor cells (HSPC) in 10 L single-use bioreactors (1). This strategy could be used to mass produce neutrophils and generate sufficient cell numbers to allow decisive clinical trials of neutrophil transfusion. We present a bioprocess model for neutrophil production at relevant clinical-scale. We evaluated two production scenarios, and the impact on cost of goods (COG) of multiple model parameters including cell yield, materials costs, and process duration. The most significant contributors to cost were consumables and raw materials, including the cost of procuring HSPC-containing umbilical cord blood. The model indicates that the most cost-efficient culture volume (batch size) is ~100 L in a single bioreactor. This study serves as a framework for decision-making and optimization strategies when contemplating the production of clinical quantities of cells for allogeneic therapy.
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spelling pubmed-64055172019-03-15 Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation Torres-Acosta, Mario A. Harrison, Richard P. Csaszar, Elizabeth Rito-Palomares, Marco Brunck, Marion E. G. Front Med (Lausanne) Medicine Neutropenia is a common side-effect of acute myeloid leukemia (AML) chemotherapy characterized by a critical drop in neutrophil blood concentration. Neutropenic patients are prone to infections, experience poorer clinical outcomes, and require expensive medical care. Although transfusions of donor neutrophils are a logical solution to neutropenia, this approach has not gained clinical traction, primarily due to challenges associated with obtaining sufficiently large numbers of neutrophils from donors whilst logistically managing their extremely short shelf-life. A protocol has been developed that produces clinical-scale quantities of neutrophils from hematopoietic stem and progenitor cells (HSPC) in 10 L single-use bioreactors (1). This strategy could be used to mass produce neutrophils and generate sufficient cell numbers to allow decisive clinical trials of neutrophil transfusion. We present a bioprocess model for neutrophil production at relevant clinical-scale. We evaluated two production scenarios, and the impact on cost of goods (COG) of multiple model parameters including cell yield, materials costs, and process duration. The most significant contributors to cost were consumables and raw materials, including the cost of procuring HSPC-containing umbilical cord blood. The model indicates that the most cost-efficient culture volume (batch size) is ~100 L in a single bioreactor. This study serves as a framework for decision-making and optimization strategies when contemplating the production of clinical quantities of cells for allogeneic therapy. Frontiers Media S.A. 2019-03-01 /pmc/articles/PMC6405517/ /pubmed/30881955 http://dx.doi.org/10.3389/fmed.2019.00021 Text en Copyright © 2019 Torres-Acosta, Harrison, Csaszar, Rito-Palomares and Brunck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Torres-Acosta, Mario A.
Harrison, Richard P.
Csaszar, Elizabeth
Rito-Palomares, Marco
Brunck, Marion E. G.
Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title_full Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title_fullStr Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title_full_unstemmed Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title_short Ex vivo Manufactured Neutrophils for Treatment of Neutropenia—A Process Economic Evaluation
title_sort ex vivo manufactured neutrophils for treatment of neutropenia—a process economic evaluation
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405517/
https://www.ncbi.nlm.nih.gov/pubmed/30881955
http://dx.doi.org/10.3389/fmed.2019.00021
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