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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7177280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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