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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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Detalles Bibliográficos
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
Descripción
Sumario: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.