Cargando…

Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines

The COVID-19-inducing virus, SARS-CoV2, is likely to remain a threat to human health unless efficient drugs or vaccines become available. Given the extent of the current pandemic (people in over one hundred countries infected) and its disastrous effect on world economy (associated with limitations o...

Descripción completa

Detalles Bibliográficos
Autores principales: Busquet, Francois, Hartung, Thomas, Pallocca, Giorgia, Rovida, Costanza, Leist, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245508/
https://www.ncbi.nlm.nih.gov/pubmed/32447523
http://dx.doi.org/10.1007/s00204-020-02787-2
_version_ 1783537769158541312
author Busquet, Francois
Hartung, Thomas
Pallocca, Giorgia
Rovida, Costanza
Leist, Marcel
author_facet Busquet, Francois
Hartung, Thomas
Pallocca, Giorgia
Rovida, Costanza
Leist, Marcel
author_sort Busquet, Francois
collection PubMed
description The COVID-19-inducing virus, SARS-CoV2, is likely to remain a threat to human health unless efficient drugs or vaccines become available. Given the extent of the current pandemic (people in over one hundred countries infected) and its disastrous effect on world economy (associated with limitations of human rights), speedy drug discovery is critical. In this situation, past investments into the development of new (animal-free) approach methods (NAM) for drug safety, efficacy, and quality evaluation can be leveraged. For this, we provide an overview of repurposing ideas to shortcut drug development times. Animal-based testing would be too lengthy, and it largely fails, when a pathogen is species-specific or if the desired drug is based on specific features of human biology. Fortunately, industry has already largely shifted to NAM, and some public funding programs have advanced the development of animal-free technologies. For instance, NAM can predict genotoxicity (a major aspect of carcinogenicity) within days, human antibodies targeting virus epitopes can be generated in molecular biology laboratories within weeks, and various human cell-based organoids are available to test virus infectivity and the biological processes controlling them. The European Medicines Agency (EMA) has formed an expert group to pave the way for the use of such approaches for accelerated drug development. This situation illustrates the importance of diversification in drug discovery strategies and clearly shows the shortcomings of an approach that invests 95% of resources into a single technology (animal experimentation) in the face of challenges that require alternative approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00204-020-02787-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-7245508
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-72455082020-05-26 Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines Busquet, Francois Hartung, Thomas Pallocca, Giorgia Rovida, Costanza Leist, Marcel Arch Toxicol Guest Editorial The COVID-19-inducing virus, SARS-CoV2, is likely to remain a threat to human health unless efficient drugs or vaccines become available. Given the extent of the current pandemic (people in over one hundred countries infected) and its disastrous effect on world economy (associated with limitations of human rights), speedy drug discovery is critical. In this situation, past investments into the development of new (animal-free) approach methods (NAM) for drug safety, efficacy, and quality evaluation can be leveraged. For this, we provide an overview of repurposing ideas to shortcut drug development times. Animal-based testing would be too lengthy, and it largely fails, when a pathogen is species-specific or if the desired drug is based on specific features of human biology. Fortunately, industry has already largely shifted to NAM, and some public funding programs have advanced the development of animal-free technologies. For instance, NAM can predict genotoxicity (a major aspect of carcinogenicity) within days, human antibodies targeting virus epitopes can be generated in molecular biology laboratories within weeks, and various human cell-based organoids are available to test virus infectivity and the biological processes controlling them. The European Medicines Agency (EMA) has formed an expert group to pave the way for the use of such approaches for accelerated drug development. This situation illustrates the importance of diversification in drug discovery strategies and clearly shows the shortcomings of an approach that invests 95% of resources into a single technology (animal experimentation) in the face of challenges that require alternative approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00204-020-02787-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-05-23 2020 /pmc/articles/PMC7245508/ /pubmed/32447523 http://dx.doi.org/10.1007/s00204-020-02787-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Guest Editorial
Busquet, Francois
Hartung, Thomas
Pallocca, Giorgia
Rovida, Costanza
Leist, Marcel
Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title_full Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title_fullStr Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title_full_unstemmed Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title_short Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines
title_sort harnessing the power of novel animal-free test methods for the development of covid-19 drugs and vaccines
topic Guest Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245508/
https://www.ncbi.nlm.nih.gov/pubmed/32447523
http://dx.doi.org/10.1007/s00204-020-02787-2
work_keys_str_mv AT busquetfrancois harnessingthepowerofnovelanimalfreetestmethodsforthedevelopmentofcovid19drugsandvaccines
AT hartungthomas harnessingthepowerofnovelanimalfreetestmethodsforthedevelopmentofcovid19drugsandvaccines
AT palloccagiorgia harnessingthepowerofnovelanimalfreetestmethodsforthedevelopmentofcovid19drugsandvaccines
AT rovidacostanza harnessingthepowerofnovelanimalfreetestmethodsforthedevelopmentofcovid19drugsandvaccines
AT leistmarcel harnessingthepowerofnovelanimalfreetestmethodsforthedevelopmentofcovid19drugsandvaccines