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3D engineered tissue models for studying human-specific infectious viral diseases

Viral infections cause damage to various organ systems by inducing organ-specific symptoms or systemic multi-organ damage. Depending on the infection route and virus type, infectious diseases are classified as respiratory, nervous, immune, digestive, or skin infections. Since these infectious diseas...

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Autores principales: Hwang, Kyeong Seob, Seo, Eun U, Choi, Nakwon, Kim, Jongbaeg, Kim, Hong Nam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519398/
https://www.ncbi.nlm.nih.gov/pubmed/36204281
http://dx.doi.org/10.1016/j.bioactmat.2022.09.010
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author Hwang, Kyeong Seob
Seo, Eun U
Choi, Nakwon
Kim, Jongbaeg
Kim, Hong Nam
author_facet Hwang, Kyeong Seob
Seo, Eun U
Choi, Nakwon
Kim, Jongbaeg
Kim, Hong Nam
author_sort Hwang, Kyeong Seob
collection PubMed
description Viral infections cause damage to various organ systems by inducing organ-specific symptoms or systemic multi-organ damage. Depending on the infection route and virus type, infectious diseases are classified as respiratory, nervous, immune, digestive, or skin infections. Since these infectious diseases can widely spread in the community and their catastrophic effects are severe, identification of their causative agent and mechanisms underlying their pathogenesis is an urgent necessity. Although infection-associated mechanisms have been studied in two-dimensional (2D) cell culture models and animal models, they have shown limitations in organ-specific or human-associated pathogenesis, and the development of a human-organ-mimetic system is required. Recently, three-dimensional (3D) engineered tissue models, which can present human organ-like physiology in terms of the 3D structure, utilization of human-originated cells, recapitulation of physiological stimuli, and tight cell–cell interactions, were developed. Furthermore, recent studies have shown that these models can recapitulate infection-associated pathologies. In this review, we summarized the recent advances in 3D engineered tissue models that mimic organ-specific viral infections. First, we briefly described the limitations of the current 2D and animal models in recapitulating human-specific viral infection pathology. Next, we provided an overview of recently reported viral infection models, focusing particularly on organ-specific infection pathologies. Finally, a future perspective that must be pursued to reconstitute more human-specific infectious diseases is presented.
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spelling pubmed-95193982022-10-05 3D engineered tissue models for studying human-specific infectious viral diseases Hwang, Kyeong Seob Seo, Eun U Choi, Nakwon Kim, Jongbaeg Kim, Hong Nam Bioact Mater Review Article Viral infections cause damage to various organ systems by inducing organ-specific symptoms or systemic multi-organ damage. Depending on the infection route and virus type, infectious diseases are classified as respiratory, nervous, immune, digestive, or skin infections. Since these infectious diseases can widely spread in the community and their catastrophic effects are severe, identification of their causative agent and mechanisms underlying their pathogenesis is an urgent necessity. Although infection-associated mechanisms have been studied in two-dimensional (2D) cell culture models and animal models, they have shown limitations in organ-specific or human-associated pathogenesis, and the development of a human-organ-mimetic system is required. Recently, three-dimensional (3D) engineered tissue models, which can present human organ-like physiology in terms of the 3D structure, utilization of human-originated cells, recapitulation of physiological stimuli, and tight cell–cell interactions, were developed. Furthermore, recent studies have shown that these models can recapitulate infection-associated pathologies. In this review, we summarized the recent advances in 3D engineered tissue models that mimic organ-specific viral infections. First, we briefly described the limitations of the current 2D and animal models in recapitulating human-specific viral infection pathology. Next, we provided an overview of recently reported viral infection models, focusing particularly on organ-specific infection pathologies. Finally, a future perspective that must be pursued to reconstitute more human-specific infectious diseases is presented. KeAi Publishing 2022-09-22 /pmc/articles/PMC9519398/ /pubmed/36204281 http://dx.doi.org/10.1016/j.bioactmat.2022.09.010 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Hwang, Kyeong Seob
Seo, Eun U
Choi, Nakwon
Kim, Jongbaeg
Kim, Hong Nam
3D engineered tissue models for studying human-specific infectious viral diseases
title 3D engineered tissue models for studying human-specific infectious viral diseases
title_full 3D engineered tissue models for studying human-specific infectious viral diseases
title_fullStr 3D engineered tissue models for studying human-specific infectious viral diseases
title_full_unstemmed 3D engineered tissue models for studying human-specific infectious viral diseases
title_short 3D engineered tissue models for studying human-specific infectious viral diseases
title_sort 3d engineered tissue models for studying human-specific infectious viral diseases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519398/
https://www.ncbi.nlm.nih.gov/pubmed/36204281
http://dx.doi.org/10.1016/j.bioactmat.2022.09.010
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