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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Main Authors: Nathan Lawko, Charlie Plaskasovitis, Carling Stokes, Laila Abelseth, Ian Fraser, Ruchi Sharma, Rebecca Kirsch, Misha Hasan, Emily Abelseth, Stephanie M. Willerth
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Materials
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmats.2021.631373/full
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spelling 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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