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


Journal

Archives of toxicology
ISSN: 1432-0738
Titre abrégé: Arch Toxicol
Pays: Germany
ID NLM: 0417615

Informations de publication

Date de publication:
06 2020
Historique:
received: 29 04 2020
accepted: 18 05 2020
pubmed: 25 5 2020
medline: 24 6 2020
entrez: 25 5 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32447523
doi: 10.1007/s00204-020-02787-2
pii: 10.1007/s00204-020-02787-2
pmc: PMC7245508
doi:

Substances chimiques

Antiviral Agents 0
COVID-19 Vaccines 0
Viral Vaccines 0

Types de publication

Editorial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2263-2272

Subventions

Organisme : Horizon 2020 Framework Programme
ID : 681002
Pays : International
Organisme : Horizon 2020 Framework Programme
ID : 825759
Pays : International

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Auteurs

Francois Busquet (F)

CAAT-Europe at the University of Konstanz, 78457, Konstanz, Germany.
ALTERTOX, 1000, Brussels, Belgium.

Thomas Hartung (T)

CAAT-Europe at the University of Konstanz, 78457, Konstanz, Germany.
CAAT, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, 21287, USA.

Giorgia Pallocca (G)

CAAT-Europe at the University of Konstanz, 78457, Konstanz, Germany.

Costanza Rovida (C)

CAAT-Europe at the University of Konstanz, 78457, Konstanz, Germany.

Marcel Leist (M)

CAAT-Europe at the University of Konstanz, 78457, Konstanz, Germany. marcel.leist@uni-konstanz.de.
In Vitro Toxicology and Biomedicine, Department Inaugurated By the Doerenkamp-Zbinden Foundation, University of Konstanz, 78457, Konstanz, Germany. marcel.leist@uni-konstanz.de.

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