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

被引:7
|
作者
Hwang, Kyeong Seob [1 ,2 ]
Seo, Eun U. [1 ,4 ]
Choi, Nakwon [1 ,5 ]
Kim, Jongbaeg [2 ]
Kim, Hong Nam [1 ,3 ,4 ]
机构
[1] Korea Inst Sci & Technol KIST, Brain Sci Inst, Seoul 02792, South Korea
[2] Yonsei Univ, Sch Mech Engn, Seoul 03722, South Korea
[3] Yonsei Univ, Yonsei KIST Convergence Res Inst, Seoul 03722, South Korea
[4] Korea Univ Sci & Technol UST, KIST Sch, Div Biomed Sci & Technol, Seoul 02792, South Korea
[5] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
3D engineered tissue model; Infectious viral disease; Infection route; Pathology; Invivo-mimicking; RESPIRATORY SYNCYTIAL VIRUS; HUMAN-PAPILLOMAVIRUS INFECTION; HUMAN NOROVIRUS INFECTION; NEURAL PROGENITOR CELLS; HERPES-SIMPLEX VIRUS-1; MOUSE MODEL; JAPANESE ENCEPHALITIS; CEREBRAL ORGANOIDS; CHIKUNGUNYA VIRUS; INFLUENZA-VIRUS;
D O I
10.1016/j.bioactmat.2022.09.010
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 com-munity and their catastrophic effects are severe, identification of their causative agent and mechanisms un-derlying 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.
引用
收藏
页码:576 / 594
页数:19
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