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mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles
In the quest for a formidable weapon against the SARS-CoV-2 pandemic, mRNA therapeutics have stolen the spotlight. mRNA vaccines are a prime example of the benefits of mRNA approaches towards a broad array of clinical entities and druggable targets. Amongst these benefits is the rapid cycle “from de...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773365/ https://www.ncbi.nlm.nih.gov/pubmed/35052730 http://dx.doi.org/10.3390/biomedicines10010050 |
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author | Ouranidis, Andreas Vavilis, Theofanis Mandala, Evdokia Davidopoulou, Christina Stamoula, Eleni Markopoulou, Catherine K. Karagianni, Anna Kachrimanis, Kyriakos |
author_facet | Ouranidis, Andreas Vavilis, Theofanis Mandala, Evdokia Davidopoulou, Christina Stamoula, Eleni Markopoulou, Catherine K. Karagianni, Anna Kachrimanis, Kyriakos |
author_sort | Ouranidis, Andreas |
collection | PubMed |
description | In the quest for a formidable weapon against the SARS-CoV-2 pandemic, mRNA therapeutics have stolen the spotlight. mRNA vaccines are a prime example of the benefits of mRNA approaches towards a broad array of clinical entities and druggable targets. Amongst these benefits is the rapid cycle “from design to production” of an mRNA product compared to their peptide counterparts, the mutability of the production line should another target be chosen, the side-stepping of safety issues posed by DNA therapeutics being permanently integrated into the transfected cell’s genome and the controlled precision over the translated peptides. Furthermore, mRNA applications are versatile: apart from vaccines it can be used as a replacement therapy, even to create chimeric antigen receptor T-cells or reprogram somatic cells. Still, the sudden global demand for mRNA has highlighted the shortcomings in its industrial production as well as its formulation, efficacy and applicability. Continuous, smart mRNA manufacturing 4.0 technologies have been recently proposed to address such challenges. In this work, we examine the lab and upscaled production of mRNA therapeutics, the mRNA modifications proposed that increase its efficacy and lower its immunogenicity, the vectors available for delivery and the stability considerations concerning long-term storage. |
format | Online Article Text |
id | pubmed-8773365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87733652022-01-21 mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles Ouranidis, Andreas Vavilis, Theofanis Mandala, Evdokia Davidopoulou, Christina Stamoula, Eleni Markopoulou, Catherine K. Karagianni, Anna Kachrimanis, Kyriakos Biomedicines Review In the quest for a formidable weapon against the SARS-CoV-2 pandemic, mRNA therapeutics have stolen the spotlight. mRNA vaccines are a prime example of the benefits of mRNA approaches towards a broad array of clinical entities and druggable targets. Amongst these benefits is the rapid cycle “from design to production” of an mRNA product compared to their peptide counterparts, the mutability of the production line should another target be chosen, the side-stepping of safety issues posed by DNA therapeutics being permanently integrated into the transfected cell’s genome and the controlled precision over the translated peptides. Furthermore, mRNA applications are versatile: apart from vaccines it can be used as a replacement therapy, even to create chimeric antigen receptor T-cells or reprogram somatic cells. Still, the sudden global demand for mRNA has highlighted the shortcomings in its industrial production as well as its formulation, efficacy and applicability. Continuous, smart mRNA manufacturing 4.0 technologies have been recently proposed to address such challenges. In this work, we examine the lab and upscaled production of mRNA therapeutics, the mRNA modifications proposed that increase its efficacy and lower its immunogenicity, the vectors available for delivery and the stability considerations concerning long-term storage. MDPI 2021-12-27 /pmc/articles/PMC8773365/ /pubmed/35052730 http://dx.doi.org/10.3390/biomedicines10010050 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ouranidis, Andreas Vavilis, Theofanis Mandala, Evdokia Davidopoulou, Christina Stamoula, Eleni Markopoulou, Catherine K. Karagianni, Anna Kachrimanis, Kyriakos mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title | mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title_full | mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title_fullStr | mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title_full_unstemmed | mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title_short | mRNA Therapeutic Modalities Design, Formulation and Manufacturing under Pharma 4.0 Principles |
title_sort | mrna therapeutic modalities design, formulation and manufacturing under pharma 4.0 principles |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773365/ https://www.ncbi.nlm.nih.gov/pubmed/35052730 http://dx.doi.org/10.3390/biomedicines10010050 |
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