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Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction

We previously demonstrated that intracardiac delivery of autologous peripheral blood‐derived CD34(+) stem cells (SCs), mobilized by granulocyte‐colony stimulating factor (G‐CSF) and collected by leukapheresis after myocardial infarction, structurally and functionally repaired the damaged myocardial...

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Autores principales: Saucourt, Claire, Vogt, Sandrine, Merlin, Amandine, Valat, Christophe, Criquet, Anthony, Harmand, Laurence, Birebent, Brigitte, Rouard, Hélène, Himmelspach, Christian, Jeandidier, Éric, Chartois‐Leauté, Anne‐Gaële, Derenne, Sophie, Koehl, Laurence, Salem, Joe‐Elie, Hulot, Jean‐Sébastien, Tancredi, Céline, Aries, Anne, Judé, Sébastien, Martel, Eric, Richard, Serge, Douay, Luc, Hénon, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646685/
https://www.ncbi.nlm.nih.gov/pubmed/31037857
http://dx.doi.org/10.1002/sctm.17-0277
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author Saucourt, Claire
Vogt, Sandrine
Merlin, Amandine
Valat, Christophe
Criquet, Anthony
Harmand, Laurence
Birebent, Brigitte
Rouard, Hélène
Himmelspach, Christian
Jeandidier, Éric
Chartois‐Leauté, Anne‐Gaële
Derenne, Sophie
Koehl, Laurence
Salem, Joe‐Elie
Hulot, Jean‐Sébastien
Tancredi, Céline
Aries, Anne
Judé, Sébastien
Martel, Eric
Richard, Serge
Douay, Luc
Hénon, Philippe
author_facet Saucourt, Claire
Vogt, Sandrine
Merlin, Amandine
Valat, Christophe
Criquet, Anthony
Harmand, Laurence
Birebent, Brigitte
Rouard, Hélène
Himmelspach, Christian
Jeandidier, Éric
Chartois‐Leauté, Anne‐Gaële
Derenne, Sophie
Koehl, Laurence
Salem, Joe‐Elie
Hulot, Jean‐Sébastien
Tancredi, Céline
Aries, Anne
Judé, Sébastien
Martel, Eric
Richard, Serge
Douay, Luc
Hénon, Philippe
author_sort Saucourt, Claire
collection PubMed
description We previously demonstrated that intracardiac delivery of autologous peripheral blood‐derived CD34(+) stem cells (SCs), mobilized by granulocyte‐colony stimulating factor (G‐CSF) and collected by leukapheresis after myocardial infarction, structurally and functionally repaired the damaged myocardial area. When used for cardiac indication, CD34(+) cells are now considered as Advanced Therapy Medicinal Products (ATMPs). We have industrialized their production by developing an automated device for ex vivo CD34(+)‐SC expansion, starting from a whole blood (WB) sample. Blood samples were collected from healthy donors after G‐CSF mobilization. Manufacturing procedures included: (a) isolation of total nuclear cells, (b) CD34(+) immunoselection, (c) expansion and cell culture recovery in the device, and (d) expanded CD34(+) cell immunoselection and formulation. The assessment of CD34(+) cell counts, viability, and immunophenotype and sterility tests were performed as quality tests. We established graft acceptance criteria and performed validation processes in three cell therapy centers. 59.4 × 10(6) ± 36.8 × 10(6) viable CD34(+) cells were reproducibly generated as the final product from 220 ml WB containing 17.1 × 10(6) ± 8.1 × 10(6) viable CD34(+) cells. CD34(+) identity, genetic stability, and telomere length were consistent with those of basal CD34(+) cells. Gram staining and mycoplasma and endotoxin analyses were negative in all cases. We confirmed the therapeutic efficacy of both CD34(+)‐cell categories in experimental acute myocardial infarct (AMI) in immunodeficient rats during preclinical studies. This reproducible, automated, and standardized expansion process produces high numbers of CD34(+) cells corresponding to the approved ATMP and paves the way for a phase I/IIb study in AMI, which is currently recruiting patients. stem cells translational medicine 2019;8:822&832
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spelling pubmed-66466852019-07-31 Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction Saucourt, Claire Vogt, Sandrine Merlin, Amandine Valat, Christophe Criquet, Anthony Harmand, Laurence Birebent, Brigitte Rouard, Hélène Himmelspach, Christian Jeandidier, Éric Chartois‐Leauté, Anne‐Gaële Derenne, Sophie Koehl, Laurence Salem, Joe‐Elie Hulot, Jean‐Sébastien Tancredi, Céline Aries, Anne Judé, Sébastien Martel, Eric Richard, Serge Douay, Luc Hénon, Philippe Stem Cells Transl Med Manufacturing for Regenerative Medicine We previously demonstrated that intracardiac delivery of autologous peripheral blood‐derived CD34(+) stem cells (SCs), mobilized by granulocyte‐colony stimulating factor (G‐CSF) and collected by leukapheresis after myocardial infarction, structurally and functionally repaired the damaged myocardial area. When used for cardiac indication, CD34(+) cells are now considered as Advanced Therapy Medicinal Products (ATMPs). We have industrialized their production by developing an automated device for ex vivo CD34(+)‐SC expansion, starting from a whole blood (WB) sample. Blood samples were collected from healthy donors after G‐CSF mobilization. Manufacturing procedures included: (a) isolation of total nuclear cells, (b) CD34(+) immunoselection, (c) expansion and cell culture recovery in the device, and (d) expanded CD34(+) cell immunoselection and formulation. The assessment of CD34(+) cell counts, viability, and immunophenotype and sterility tests were performed as quality tests. We established graft acceptance criteria and performed validation processes in three cell therapy centers. 59.4 × 10(6) ± 36.8 × 10(6) viable CD34(+) cells were reproducibly generated as the final product from 220 ml WB containing 17.1 × 10(6) ± 8.1 × 10(6) viable CD34(+) cells. CD34(+) identity, genetic stability, and telomere length were consistent with those of basal CD34(+) cells. Gram staining and mycoplasma and endotoxin analyses were negative in all cases. We confirmed the therapeutic efficacy of both CD34(+)‐cell categories in experimental acute myocardial infarct (AMI) in immunodeficient rats during preclinical studies. This reproducible, automated, and standardized expansion process produces high numbers of CD34(+) cells corresponding to the approved ATMP and paves the way for a phase I/IIb study in AMI, which is currently recruiting patients. stem cells translational medicine 2019;8:822&832 John Wiley & Sons, Inc. 2019-04-29 /pmc/articles/PMC6646685/ /pubmed/31037857 http://dx.doi.org/10.1002/sctm.17-0277 Text en © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Manufacturing for Regenerative Medicine
Saucourt, Claire
Vogt, Sandrine
Merlin, Amandine
Valat, Christophe
Criquet, Anthony
Harmand, Laurence
Birebent, Brigitte
Rouard, Hélène
Himmelspach, Christian
Jeandidier, Éric
Chartois‐Leauté, Anne‐Gaële
Derenne, Sophie
Koehl, Laurence
Salem, Joe‐Elie
Hulot, Jean‐Sébastien
Tancredi, Céline
Aries, Anne
Judé, Sébastien
Martel, Eric
Richard, Serge
Douay, Luc
Hénon, Philippe
Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title_full Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title_fullStr Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title_full_unstemmed Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title_short Design and Validation of an Automated Process for the Expansion of Peripheral Blood‐Derived CD34(+) Cells for Clinical Use After Myocardial Infarction
title_sort design and validation of an automated process for the expansion of peripheral blood‐derived cd34(+) cells for clinical use after myocardial infarction
topic Manufacturing for Regenerative Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646685/
https://www.ncbi.nlm.nih.gov/pubmed/31037857
http://dx.doi.org/10.1002/sctm.17-0277
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