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Development of an in vitro potency assay for human skeletal muscle derived cells

BACKGROUND: Potency is a quantitative measure of the desired biological function of an advanced therapy medicinal product (ATMP) and is a prerequisite for market approval application (MAA). To assess the potency of human skeletal muscle-derived cells (SMDCs), which are currently investigated in clin...

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Autores principales: Thurner, Marco, Asim, Faheem, Garczarczyk-Asim, Dorota, Janke, Katrin, Deutsch, Martin, Margreiter, Eva, Troppmair, Jakob, Marksteiner, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864011/
https://www.ncbi.nlm.nih.gov/pubmed/29566057
http://dx.doi.org/10.1371/journal.pone.0194561
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author Thurner, Marco
Asim, Faheem
Garczarczyk-Asim, Dorota
Janke, Katrin
Deutsch, Martin
Margreiter, Eva
Troppmair, Jakob
Marksteiner, Rainer
author_facet Thurner, Marco
Asim, Faheem
Garczarczyk-Asim, Dorota
Janke, Katrin
Deutsch, Martin
Margreiter, Eva
Troppmair, Jakob
Marksteiner, Rainer
author_sort Thurner, Marco
collection PubMed
description BACKGROUND: Potency is a quantitative measure of the desired biological function of an advanced therapy medicinal product (ATMP) and is a prerequisite for market approval application (MAA). To assess the potency of human skeletal muscle-derived cells (SMDCs), which are currently investigated in clinical trials for the regeneration of skeletal muscle defects, we evaluated acetylcholinesterase (AChE), which is expressed in skeletal muscle and nervous tissue of all mammals. METHODS: CD56(+) SMDCs were separated from CD56(-) SMDCs by magnetic activated cell sorting (MACS) and both differentiated in skeletal muscle differentiation medium. AChE activity of in vitro differentiated SMDCs was correlated with CD56 expression, fusion index, cell number, cell doubling numbers, differentiation markers and compared to the clinical efficacy in patients treated with SMDCs against fecal incontinence. RESULTS: CD56(-) SMDCs did not form multinucleated myotubes and remained low in AChE activity during differentiation. CD56(+) SMDCs generated myotubes and increased in AChE activity during differentiation. AChE activity was found to accurately reflect the number of CD56(+) SMDCs in culture, their fusion competence, and cell doubling number. In patients with fecal incontinence responding to SMDCs treatment, the improvement of clinical symptoms was positively linked with the AChE activity of the SMDCs injected. DISCUSSION: AChE activity was found to truly reflect the in vitro differentiation status of SMDCs and to be superior to the mere use of surface markers as it reflects not only the number of myogenic SMDCs in culture but also their fusion competence and population doubling number, thus combining cell quality and quantification of the expected mode of action (MoA) of SMDCs. Moreover, the successful in vitro validation of the assay proves its suitability for routine use. Most convincingly, our results demonstrate a link between clinical efficacy and the AChE activity of the SMDCs preparations used for the treatment of fecal incontinence. Thus, we recommend using AChE activity of in vitro differentiated SMDCs as a potency measure in end stage (phase III) clinical trials using SMDCs for skeletal muscle regeneration and subsequent market approval application (MAA).
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spelling pubmed-58640112018-03-28 Development of an in vitro potency assay for human skeletal muscle derived cells Thurner, Marco Asim, Faheem Garczarczyk-Asim, Dorota Janke, Katrin Deutsch, Martin Margreiter, Eva Troppmair, Jakob Marksteiner, Rainer PLoS One Research Article BACKGROUND: Potency is a quantitative measure of the desired biological function of an advanced therapy medicinal product (ATMP) and is a prerequisite for market approval application (MAA). To assess the potency of human skeletal muscle-derived cells (SMDCs), which are currently investigated in clinical trials for the regeneration of skeletal muscle defects, we evaluated acetylcholinesterase (AChE), which is expressed in skeletal muscle and nervous tissue of all mammals. METHODS: CD56(+) SMDCs were separated from CD56(-) SMDCs by magnetic activated cell sorting (MACS) and both differentiated in skeletal muscle differentiation medium. AChE activity of in vitro differentiated SMDCs was correlated with CD56 expression, fusion index, cell number, cell doubling numbers, differentiation markers and compared to the clinical efficacy in patients treated with SMDCs against fecal incontinence. RESULTS: CD56(-) SMDCs did not form multinucleated myotubes and remained low in AChE activity during differentiation. CD56(+) SMDCs generated myotubes and increased in AChE activity during differentiation. AChE activity was found to accurately reflect the number of CD56(+) SMDCs in culture, their fusion competence, and cell doubling number. In patients with fecal incontinence responding to SMDCs treatment, the improvement of clinical symptoms was positively linked with the AChE activity of the SMDCs injected. DISCUSSION: AChE activity was found to truly reflect the in vitro differentiation status of SMDCs and to be superior to the mere use of surface markers as it reflects not only the number of myogenic SMDCs in culture but also their fusion competence and population doubling number, thus combining cell quality and quantification of the expected mode of action (MoA) of SMDCs. Moreover, the successful in vitro validation of the assay proves its suitability for routine use. Most convincingly, our results demonstrate a link between clinical efficacy and the AChE activity of the SMDCs preparations used for the treatment of fecal incontinence. Thus, we recommend using AChE activity of in vitro differentiated SMDCs as a potency measure in end stage (phase III) clinical trials using SMDCs for skeletal muscle regeneration and subsequent market approval application (MAA). Public Library of Science 2018-03-22 /pmc/articles/PMC5864011/ /pubmed/29566057 http://dx.doi.org/10.1371/journal.pone.0194561 Text en © 2018 Thurner et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Thurner, Marco
Asim, Faheem
Garczarczyk-Asim, Dorota
Janke, Katrin
Deutsch, Martin
Margreiter, Eva
Troppmair, Jakob
Marksteiner, Rainer
Development of an in vitro potency assay for human skeletal muscle derived cells
title Development of an in vitro potency assay for human skeletal muscle derived cells
title_full Development of an in vitro potency assay for human skeletal muscle derived cells
title_fullStr Development of an in vitro potency assay for human skeletal muscle derived cells
title_full_unstemmed Development of an in vitro potency assay for human skeletal muscle derived cells
title_short Development of an in vitro potency assay for human skeletal muscle derived cells
title_sort development of an in vitro potency assay for human skeletal muscle derived cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864011/
https://www.ncbi.nlm.nih.gov/pubmed/29566057
http://dx.doi.org/10.1371/journal.pone.0194561
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