Cargando…

The challenge of developing human 3D organoids into medicines

The capacity of organoids to generate complex 3D structures resembling organs is revolutionizing the fields of developmental and stem cell biology. We are currently establishing the foundations for translational applications of organoids such as drug screening, personalized medicine and launching th...

Descripción completa

Detalles Bibliográficos
Autores principales: Vives, Joaquim, Batlle-Morera, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055107/
https://www.ncbi.nlm.nih.gov/pubmed/32127036
http://dx.doi.org/10.1186/s13287-020-1586-1
_version_ 1783503310369587200
author Vives, Joaquim
Batlle-Morera, Laura
author_facet Vives, Joaquim
Batlle-Morera, Laura
author_sort Vives, Joaquim
collection PubMed
description The capacity of organoids to generate complex 3D structures resembling organs is revolutionizing the fields of developmental and stem cell biology. We are currently establishing the foundations for translational applications of organoids such as drug screening, personalized medicine and launching the future of cell therapy using organoids. However, clinical translation of organoids into cell replacement therapies is halted due to (A) a few preclinical studies demonstrating their efficacy and (B) the lack of robust, reproducible, and scalable methods of production in compliance with current pharmaceutical standards. In this issue of Stem Cell Research & Therapy [ref], Dossena and collaborators present a validated bioprocess design for large-scale production of human pancreatic organoids from cadaveric tissue in accordance with current good manufacturing practice. The authors also propose a set of specifications of starting materials and critical quality attributes of final products that are of interest to other developments provided that this type of medicines are different than any other medicinal product due to their complex composition and living nature of the active ingredient. Although large-scale production of functional cells secreting insulin is still a challenge, the development of methods such as the one presented by Dossena and collaborators contributes to move toward clinical use of organoids in the treatment of type 1 diabetes and opens avenues for future clinical use of organoids in degenerative pathologies.
format Online
Article
Text
id pubmed-7055107
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-70551072020-03-10 The challenge of developing human 3D organoids into medicines Vives, Joaquim Batlle-Morera, Laura Stem Cell Res Ther Commentary The capacity of organoids to generate complex 3D structures resembling organs is revolutionizing the fields of developmental and stem cell biology. We are currently establishing the foundations for translational applications of organoids such as drug screening, personalized medicine and launching the future of cell therapy using organoids. However, clinical translation of organoids into cell replacement therapies is halted due to (A) a few preclinical studies demonstrating their efficacy and (B) the lack of robust, reproducible, and scalable methods of production in compliance with current pharmaceutical standards. In this issue of Stem Cell Research & Therapy [ref], Dossena and collaborators present a validated bioprocess design for large-scale production of human pancreatic organoids from cadaveric tissue in accordance with current good manufacturing practice. The authors also propose a set of specifications of starting materials and critical quality attributes of final products that are of interest to other developments provided that this type of medicines are different than any other medicinal product due to their complex composition and living nature of the active ingredient. Although large-scale production of functional cells secreting insulin is still a challenge, the development of methods such as the one presented by Dossena and collaborators contributes to move toward clinical use of organoids in the treatment of type 1 diabetes and opens avenues for future clinical use of organoids in degenerative pathologies. BioMed Central 2020-03-04 /pmc/articles/PMC7055107/ /pubmed/32127036 http://dx.doi.org/10.1186/s13287-020-1586-1 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Vives, Joaquim
Batlle-Morera, Laura
The challenge of developing human 3D organoids into medicines
title The challenge of developing human 3D organoids into medicines
title_full The challenge of developing human 3D organoids into medicines
title_fullStr The challenge of developing human 3D organoids into medicines
title_full_unstemmed The challenge of developing human 3D organoids into medicines
title_short The challenge of developing human 3D organoids into medicines
title_sort challenge of developing human 3d organoids into medicines
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055107/
https://www.ncbi.nlm.nih.gov/pubmed/32127036
http://dx.doi.org/10.1186/s13287-020-1586-1
work_keys_str_mv AT vivesjoaquim thechallengeofdevelopinghuman3dorganoidsintomedicines
AT batllemoreralaura thechallengeofdevelopinghuman3dorganoidsintomedicines
AT vivesjoaquim challengeofdevelopinghuman3dorganoidsintomedicines
AT batllemoreralaura challengeofdevelopinghuman3dorganoidsintomedicines