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Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy

Human pluripotent stem cells have the potential to change the way in which human diseases are cured. Clinical-grade human embryonic stem cells and human induced pluripotent stem cells have to be created according to current good manufacturing practices and regulations. Quality and safety must be of...

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Detalles Bibliográficos
Autores principales: Rehakova, Daniela, Souralova, Tereza, Koutna, Irena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177280/
https://www.ncbi.nlm.nih.gov/pubmed/32244538
http://dx.doi.org/10.3390/ijms21072435
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author Rehakova, Daniela
Souralova, Tereza
Koutna, Irena
author_facet Rehakova, Daniela
Souralova, Tereza
Koutna, Irena
author_sort Rehakova, Daniela
collection PubMed
description Human pluripotent stem cells have the potential to change the way in which human diseases are cured. Clinical-grade human embryonic stem cells and human induced pluripotent stem cells have to be created according to current good manufacturing practices and regulations. Quality and safety must be of the highest importance when humans’ lives are at stake. With the rising number of clinical trials, there is a need for a consensus on hPSCs characterization. Here, we summarize mandatory and ′for information only′ characterization methods with release criteria for the establishment of clinical-grade hPSC lines.
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spelling pubmed-71772802020-04-28 Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy Rehakova, Daniela Souralova, Tereza Koutna, Irena Int J Mol Sci Review Human pluripotent stem cells have the potential to change the way in which human diseases are cured. Clinical-grade human embryonic stem cells and human induced pluripotent stem cells have to be created according to current good manufacturing practices and regulations. Quality and safety must be of the highest importance when humans’ lives are at stake. With the rising number of clinical trials, there is a need for a consensus on hPSCs characterization. Here, we summarize mandatory and ′for information only′ characterization methods with release criteria for the establishment of clinical-grade hPSC lines. MDPI 2020-03-31 /pmc/articles/PMC7177280/ /pubmed/32244538 http://dx.doi.org/10.3390/ijms21072435 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rehakova, Daniela
Souralova, Tereza
Koutna, Irena
Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title_full Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title_fullStr Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title_full_unstemmed Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title_short Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
title_sort clinical-grade human pluripotent stem cells for cell therapy: characterization strategy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177280/
https://www.ncbi.nlm.nih.gov/pubmed/32244538
http://dx.doi.org/10.3390/ijms21072435
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