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Organotypic human ex vivo models for coronavirus disease 2019 research and drug development
Since the discovery of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in late 2019, intense research efforts on an unprecedented scale have focused on the study of viral entry mechanisms and adaptive immunity. While the identification of angiotensin-converting enzyme 2 (ACE2) and other...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075816/ https://www.ncbi.nlm.nih.gov/pubmed/34029832 http://dx.doi.org/10.1016/j.coph.2021.04.006 |
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author | Youhanna, Sonia Wright, Shane C. Lauschke, Volker M. |
author_facet | Youhanna, Sonia Wright, Shane C. Lauschke, Volker M. |
author_sort | Youhanna, Sonia |
collection | PubMed |
description | Since the discovery of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in late 2019, intense research efforts on an unprecedented scale have focused on the study of viral entry mechanisms and adaptive immunity. While the identification of angiotensin-converting enzyme 2 (ACE2) and other co-receptors has elucidated the molecular and structural basis for viral entry, the pathobiological mechanisms of SARS-CoV-2 in human tissues are less understood. Recent advances in bioengineering have opened opportunities for the use of organotypic human tissue models to investigate host–virus interactions and test antiviral drug candidates in a physiological context. Although it is too early to accurately quantify the added value of these systems compared with conventional cell systems, it can be assumed that these advanced three-dimensional (3D) models contribute toward improved result translation. This mini-review summarizes recent work to study SARS-CoV-2 infection in human 3D tissue models with an emphasis on the pharmacological tools that have been developed to understand and prevent viral entry and replication. |
format | Online Article Text |
id | pubmed-8075816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Author(s). Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80758162021-04-27 Organotypic human ex vivo models for coronavirus disease 2019 research and drug development Youhanna, Sonia Wright, Shane C. Lauschke, Volker M. Curr Opin Pharmacol Article Since the discovery of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in late 2019, intense research efforts on an unprecedented scale have focused on the study of viral entry mechanisms and adaptive immunity. While the identification of angiotensin-converting enzyme 2 (ACE2) and other co-receptors has elucidated the molecular and structural basis for viral entry, the pathobiological mechanisms of SARS-CoV-2 in human tissues are less understood. Recent advances in bioengineering have opened opportunities for the use of organotypic human tissue models to investigate host–virus interactions and test antiviral drug candidates in a physiological context. Although it is too early to accurately quantify the added value of these systems compared with conventional cell systems, it can be assumed that these advanced three-dimensional (3D) models contribute toward improved result translation. This mini-review summarizes recent work to study SARS-CoV-2 infection in human 3D tissue models with an emphasis on the pharmacological tools that have been developed to understand and prevent viral entry and replication. The Author(s). Published by Elsevier Ltd. 2021-08 2021-04-27 /pmc/articles/PMC8075816/ /pubmed/34029832 http://dx.doi.org/10.1016/j.coph.2021.04.006 Text en © 2021 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Youhanna, Sonia Wright, Shane C. Lauschke, Volker M. Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title | Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title_full | Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title_fullStr | Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title_full_unstemmed | Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title_short | Organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
title_sort | organotypic human ex vivo models for coronavirus disease 2019 research and drug development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075816/ https://www.ncbi.nlm.nih.gov/pubmed/34029832 http://dx.doi.org/10.1016/j.coph.2021.04.006 |
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