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Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells

BACKGROUND: The increasing number of clinical trials for induced pluripotent stem cell (iPSC)-derived cell therapy products makes the production on clinical grade iPSC more and more relevant and necessary. Cord blood banks are an ideal source of young, HLA-typed and virus screened starting material...

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Autores principales: Álvarez-Palomo, Belén, Veiga, Anna, Raya, Angel, Codinach, Margarita, Torrents, Silvia, Ponce Verdugo, Laura, Rodriguez-Aierbe, Clara, Cuellar, Leopoldo, Alenda, Raquel, Arbona, Cristina, Hernández-Maraver, Dolores, Fusté, Cristina, Querol, Sergi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372949/
https://www.ncbi.nlm.nih.gov/pubmed/35962457
http://dx.doi.org/10.1186/s13287-022-02961-6
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author Álvarez-Palomo, Belén
Veiga, Anna
Raya, Angel
Codinach, Margarita
Torrents, Silvia
Ponce Verdugo, Laura
Rodriguez-Aierbe, Clara
Cuellar, Leopoldo
Alenda, Raquel
Arbona, Cristina
Hernández-Maraver, Dolores
Fusté, Cristina
Querol, Sergi
author_facet Álvarez-Palomo, Belén
Veiga, Anna
Raya, Angel
Codinach, Margarita
Torrents, Silvia
Ponce Verdugo, Laura
Rodriguez-Aierbe, Clara
Cuellar, Leopoldo
Alenda, Raquel
Arbona, Cristina
Hernández-Maraver, Dolores
Fusté, Cristina
Querol, Sergi
author_sort Álvarez-Palomo, Belén
collection PubMed
description BACKGROUND: The increasing number of clinical trials for induced pluripotent stem cell (iPSC)-derived cell therapy products makes the production on clinical grade iPSC more and more relevant and necessary. Cord blood banks are an ideal source of young, HLA-typed and virus screened starting material to produce HLA-homozygous iPSC lines for wide immune-compatibility allogenic cell therapy approaches. The production of such clinical grade iPSC lines (haplolines) involves particular attention to all steps since donor informed consent, cell procurement and a GMP-compliant cell isolation process. METHODS: Homozygous cord blood units were identified and quality verified before recontacting donors for informed consent. CD34+ cells were purified from the mononuclear fraction isolated in a cell processor, by magnetic microbeads labelling and separation columns. RESULTS: We obtained a median recovery of 20.0% of the collected pre-freezing CD34+, with a final product median viability of 99.1% and median purity of 83.5% of the post-thawed purified CD34+ population. CONCLUSIONS: Here we describe our own experience, from unit selection and donor reconsenting, in generating a CD34+ cell product as a starting material to produce HLA-homozygous iPSC following a cost-effective and clinical grade-compliant procedure. These CD34+ cells are the basis for the Spanish bank of haplolines envisioned to serve as a source of cell products for clinical research and therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02961-6.
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spelling pubmed-93729492022-08-12 Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells Álvarez-Palomo, Belén Veiga, Anna Raya, Angel Codinach, Margarita Torrents, Silvia Ponce Verdugo, Laura Rodriguez-Aierbe, Clara Cuellar, Leopoldo Alenda, Raquel Arbona, Cristina Hernández-Maraver, Dolores Fusté, Cristina Querol, Sergi Stem Cell Res Ther Research BACKGROUND: The increasing number of clinical trials for induced pluripotent stem cell (iPSC)-derived cell therapy products makes the production on clinical grade iPSC more and more relevant and necessary. Cord blood banks are an ideal source of young, HLA-typed and virus screened starting material to produce HLA-homozygous iPSC lines for wide immune-compatibility allogenic cell therapy approaches. The production of such clinical grade iPSC lines (haplolines) involves particular attention to all steps since donor informed consent, cell procurement and a GMP-compliant cell isolation process. METHODS: Homozygous cord blood units were identified and quality verified before recontacting donors for informed consent. CD34+ cells were purified from the mononuclear fraction isolated in a cell processor, by magnetic microbeads labelling and separation columns. RESULTS: We obtained a median recovery of 20.0% of the collected pre-freezing CD34+, with a final product median viability of 99.1% and median purity of 83.5% of the post-thawed purified CD34+ population. CONCLUSIONS: Here we describe our own experience, from unit selection and donor reconsenting, in generating a CD34+ cell product as a starting material to produce HLA-homozygous iPSC following a cost-effective and clinical grade-compliant procedure. These CD34+ cells are the basis for the Spanish bank of haplolines envisioned to serve as a source of cell products for clinical research and therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-022-02961-6. BioMed Central 2022-08-12 /pmc/articles/PMC9372949/ /pubmed/35962457 http://dx.doi.org/10.1186/s13287-022-02961-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Álvarez-Palomo, Belén
Veiga, Anna
Raya, Angel
Codinach, Margarita
Torrents, Silvia
Ponce Verdugo, Laura
Rodriguez-Aierbe, Clara
Cuellar, Leopoldo
Alenda, Raquel
Arbona, Cristina
Hernández-Maraver, Dolores
Fusté, Cristina
Querol, Sergi
Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title_full Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title_fullStr Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title_full_unstemmed Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title_short Public Cord Blood Banks as a source of starting material for clinical grade HLA-homozygous induced pluripotent stem cells
title_sort public cord blood banks as a source of starting material for clinical grade hla-homozygous induced pluripotent stem cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372949/
https://www.ncbi.nlm.nih.gov/pubmed/35962457
http://dx.doi.org/10.1186/s13287-022-02961-6
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