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

Kyeong Seob Hwang, Eun U. Seo, Nakwon Choi, Jongbaeg Kim, Hong Nam Kim

Research output: Contribution to journalReview articlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)576-594
Number of pages19
JournalBioactive Materials
Volume21
DOIs
Publication statusPublished - 2023 Mar

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant (Nos. 2021R1A2B5B02086828 and 2022M3A9B6082678 ) (H.N.K) funded by the Korean Government (MSIT) . This work was supported by Korea Environment Industry & Technology Institute (KEITI) through Technology Development Project for Biological Hazards Management in Indoor Air Program (or Project), funded by Korea Ministry of Environment (MOE) (No. 2021003370005 ). The graphical abstract was created using BioRender.com .

Publisher Copyright:
© 2022 The Authors

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Biomaterials
  • Biomedical Engineering

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