Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783437591257808896 |
---|---|
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 |
format | Online Article Text |
id | pubmed-6646685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT saucourtclaire designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT vogtsandrine designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT merlinamandine designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT valatchristophe designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT criquetanthony designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT harmandlaurence designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT birebentbrigitte designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT rouardhelene designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT himmelspachchristian designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT jeandidiereric designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT chartoisleauteannegaele designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT derennesophie designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT koehllaurence designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT salemjoeelie designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT hulotjeansebastien designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT tancrediceline designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT ariesanne designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT judesebastien designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT marteleric designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT richardserge designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT douayluc designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction AT henonphilippe designandvalidationofanautomatedprocessfortheexpansionofperipheralbloodderivedcd34cellsforclinicaluseaftermyocardialinfarction |