3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development
The recent SARS-CoV-2 outbreak has researchers working tirelessly to understand the virus' pathogenesis and develop an effective vaccine. The urgent need for rapid development and deployment of such a vaccine has illustrated the limitations of current practices, and it has highlighted the need...
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doaj-3765c6bffe744928940e5180c9d45c992021-03-22T05:15:46ZengFrontiers Media S.A.Frontiers in Materials2296-80162021-03-01810.3389/fmats.2021.6313736313733D Tissue Models as an Effective Tool for Studying Viruses and Vaccine DevelopmentNathan Lawko0Nathan Lawko1Charlie Plaskasovitis2Charlie Plaskasovitis3Carling Stokes4Carling Stokes5Laila Abelseth6Ian Fraser7Ruchi Sharma8Rebecca Kirsch9Misha Hasan10Emily Abelseth11Stephanie M. Willerth12Stephanie M. Willerth13Stephanie M. Willerth14Stephanie M. Willerth15Department of Electrical and Computer Engineering, University of Victoria, Victoria, BC, CanadaCentre for Biomedical Research, University of Victoria, Victoria, BC, CanadaDepartment of Electrical and Computer Engineering, University of Victoria, Victoria, BC, CanadaCentre for Biomedical Research, University of Victoria, Victoria, BC, CanadaCentre for Biomedical Research, University of Victoria, Victoria, BC, CanadaDepartment of Mechanical Engineering, University of Victoria, Victoria, BC, CanadaCentre for Biomedical Research, University of Victoria, Victoria, BC, CanadaDepartment of Mechanical Engineering, University of Victoria, Victoria, BC, CanadaDepartment of Mechanical Engineering, University of Victoria, Victoria, BC, CanadaDepartment of Chemistry, University of Victoria, Victoria, BC, CanadaBiomedical Engineering Program, University of Victoria, Victoria, BC, CanadaDepartment of Mechanical Engineering, University of Victoria, Victoria, BC, CanadaCentre for Biomedical Research, University of Victoria, Victoria, BC, CanadaDepartment of Mechanical Engineering, University of Victoria, Victoria, BC, CanadaBiomedical Engineering Program, University of Victoria, Victoria, BC, CanadaDivision of Medical Sciences, University of Victoria, Victoria, BC, CanadaThe recent SARS-CoV-2 outbreak has researchers working tirelessly to understand the virus' pathogenesis and develop an effective vaccine. The urgent need for rapid development and deployment of such a vaccine has illustrated the limitations of current practices, and it has highlighted the need for alternative models for early screening of such technologies. Traditional 2D cell culture does not accurately capture the effects of a physiologically relevant environment as they fail to promote appropriate cell-cell and cell-environment interactions. This inability to capture the intricacies of the in vivo microenvironment prevents 2D cell cultures from demonstrating the necessary properties of native tissues required for the standard infection mechanisms of the virus, thus contributing the high failure rate of drug discovery and vaccine development. 3D cell culture models can bridge the gap between conventional cell culture and in vivo models. Methods such as 3D bioprinting, spheroids, organoids, organ-on-chip platform, and rotating wall vessel bioreactors offer ways to produce physiologically relevant models by mimicking in vivo microarchitecture, chemical gradients, cell–cell interactions and cell–environment interactions. The field of viral biology currently uses 3D cell culture models to understand the interactions between viruses and host cells, which is crucial knowledge for vaccine development. In this review, we discuss how 3D cell culture models have been used to investigate disease pathologies for coronaviruses and other viruses such as Zika Virus, Hepatitis, and Influenza, and how they may apply to drug discovery and vaccine development.https://www.frontiersin.org/articles/10.3389/fmats.2021.631373/fullCOVID-19biomaterialstissue engineeringorganoidsantigenmicroenvironment |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nathan Lawko Nathan Lawko Charlie Plaskasovitis Charlie Plaskasovitis Carling Stokes Carling Stokes Laila Abelseth Ian Fraser Ruchi Sharma Rebecca Kirsch Misha Hasan Emily Abelseth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth |
spellingShingle |
Nathan Lawko Nathan Lawko Charlie Plaskasovitis Charlie Plaskasovitis Carling Stokes Carling Stokes Laila Abelseth Ian Fraser Ruchi Sharma Rebecca Kirsch Misha Hasan Emily Abelseth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth 3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development Frontiers in Materials COVID-19 biomaterials tissue engineering organoids antigen microenvironment |
author_facet |
Nathan Lawko Nathan Lawko Charlie Plaskasovitis Charlie Plaskasovitis Carling Stokes Carling Stokes Laila Abelseth Ian Fraser Ruchi Sharma Rebecca Kirsch Misha Hasan Emily Abelseth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth Stephanie M. Willerth |
author_sort |
Nathan Lawko |
title |
3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development |
title_short |
3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development |
title_full |
3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development |
title_fullStr |
3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development |
title_full_unstemmed |
3D Tissue Models as an Effective Tool for Studying Viruses and Vaccine Development |
title_sort |
3d tissue models as an effective tool for studying viruses and vaccine development |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Materials |
issn |
2296-8016 |
publishDate |
2021-03-01 |
description |
The recent SARS-CoV-2 outbreak has researchers working tirelessly to understand the virus' pathogenesis and develop an effective vaccine. The urgent need for rapid development and deployment of such a vaccine has illustrated the limitations of current practices, and it has highlighted the need for alternative models for early screening of such technologies. Traditional 2D cell culture does not accurately capture the effects of a physiologically relevant environment as they fail to promote appropriate cell-cell and cell-environment interactions. This inability to capture the intricacies of the in vivo microenvironment prevents 2D cell cultures from demonstrating the necessary properties of native tissues required for the standard infection mechanisms of the virus, thus contributing the high failure rate of drug discovery and vaccine development. 3D cell culture models can bridge the gap between conventional cell culture and in vivo models. Methods such as 3D bioprinting, spheroids, organoids, organ-on-chip platform, and rotating wall vessel bioreactors offer ways to produce physiologically relevant models by mimicking in vivo microarchitecture, chemical gradients, cell–cell interactions and cell–environment interactions. The field of viral biology currently uses 3D cell culture models to understand the interactions between viruses and host cells, which is crucial knowledge for vaccine development. In this review, we discuss how 3D cell culture models have been used to investigate disease pathologies for coronaviruses and other viruses such as Zika Virus, Hepatitis, and Influenza, and how they may apply to drug discovery and vaccine development. |
topic |
COVID-19 biomaterials tissue engineering organoids antigen microenvironment |
url |
https://www.frontiersin.org/articles/10.3389/fmats.2021.631373/full |
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