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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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Detalles Bibliográficos
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
Descripción
Sumario: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