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Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis

Neonatal sepsis is a major cause of death and disability in newborns. Commonly used biomarkers for diagnosis and evaluation of treatment response lack sufficient sensitivity or specificity. Additionally, new targets to treat the dysregulated immune response are needed, as are methods to effectively...

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Autores principales: Keij, Fleur M., Koch, Bjørn E. V., Lozano Vigario, Fernando, Simons, Sinno H. P., van Hasselt, Johan G. C., Taal, H. Rob, Knibbe, C. A. J., Spaink, Herman P., Reiss, Irwin K. M., Krekels, Elke H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358844/
https://www.ncbi.nlm.nih.gov/pubmed/34422320
http://dx.doi.org/10.1017/cts.2021.803
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author Keij, Fleur M.
Koch, Bjørn E. V.
Lozano Vigario, Fernando
Simons, Sinno H. P.
van Hasselt, Johan G. C.
Taal, H. Rob
Knibbe, C. A. J.
Spaink, Herman P.
Reiss, Irwin K. M.
Krekels, Elke H. J.
author_facet Keij, Fleur M.
Koch, Bjørn E. V.
Lozano Vigario, Fernando
Simons, Sinno H. P.
van Hasselt, Johan G. C.
Taal, H. Rob
Knibbe, C. A. J.
Spaink, Herman P.
Reiss, Irwin K. M.
Krekels, Elke H. J.
author_sort Keij, Fleur M.
collection PubMed
description Neonatal sepsis is a major cause of death and disability in newborns. Commonly used biomarkers for diagnosis and evaluation of treatment response lack sufficient sensitivity or specificity. Additionally, new targets to treat the dysregulated immune response are needed, as are methods to effectively screen drugs for these targets. Available research methods have hitherto not yielded the breakthroughs required to significantly improve disease outcomes, we therefore describe the potential of zebrafish (Danio rerio) larvae as preclinical model for neonatal sepsis. In biomedical research, zebrafish larvae combine the complexity of a whole organism with the convenience and high-throughput potential of in vitro methods. This paper illustrates that zebrafish exhibit an immune system that is remarkably similar to humans, both in terms of types of immune cells and signaling pathways. Moreover, the developmental state of the larval immune system is highly similar to human neonates. We provide examples of zebrafish larvae being used to study infections with pathogens commonly causing neonatal sepsis and discuss known limitations. We believe this species could expedite research into immune regulation during neonatal sepsis and may hold keys for the discovery of new biomarkers and novel treatment targets as well as for screening of targeted drug therapies.
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spelling pubmed-83588442021-08-20 Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis Keij, Fleur M. Koch, Bjørn E. V. Lozano Vigario, Fernando Simons, Sinno H. P. van Hasselt, Johan G. C. Taal, H. Rob Knibbe, C. A. J. Spaink, Herman P. Reiss, Irwin K. M. Krekels, Elke H. J. J Clin Transl Sci Review Article Neonatal sepsis is a major cause of death and disability in newborns. Commonly used biomarkers for diagnosis and evaluation of treatment response lack sufficient sensitivity or specificity. Additionally, new targets to treat the dysregulated immune response are needed, as are methods to effectively screen drugs for these targets. Available research methods have hitherto not yielded the breakthroughs required to significantly improve disease outcomes, we therefore describe the potential of zebrafish (Danio rerio) larvae as preclinical model for neonatal sepsis. In biomedical research, zebrafish larvae combine the complexity of a whole organism with the convenience and high-throughput potential of in vitro methods. This paper illustrates that zebrafish exhibit an immune system that is remarkably similar to humans, both in terms of types of immune cells and signaling pathways. Moreover, the developmental state of the larval immune system is highly similar to human neonates. We provide examples of zebrafish larvae being used to study infections with pathogens commonly causing neonatal sepsis and discuss known limitations. We believe this species could expedite research into immune regulation during neonatal sepsis and may hold keys for the discovery of new biomarkers and novel treatment targets as well as for screening of targeted drug therapies. Cambridge University Press 2021-06-18 /pmc/articles/PMC8358844/ /pubmed/34422320 http://dx.doi.org/10.1017/cts.2021.803 Text en © The Association for Clinical and Translational Science 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Keij, Fleur M.
Koch, Bjørn E. V.
Lozano Vigario, Fernando
Simons, Sinno H. P.
van Hasselt, Johan G. C.
Taal, H. Rob
Knibbe, C. A. J.
Spaink, Herman P.
Reiss, Irwin K. M.
Krekels, Elke H. J.
Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title_full Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title_fullStr Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title_full_unstemmed Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title_short Zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
title_sort zebrafish larvae as experimental model to expedite the search for new biomarkers and treatments for neonatal sepsis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358844/
https://www.ncbi.nlm.nih.gov/pubmed/34422320
http://dx.doi.org/10.1017/cts.2021.803
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