背景(考古学)
多细胞生物
大流行
冠状病毒
2019年冠状病毒病(COVID-19)
传染病(医学专业)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
计算生物学
动物模型
生物
疾病
病毒学
重症监护医学
计算机科学
医学
细胞
古生物学
病理
内分泌学
遗传学
作者
Fahimeh Shahabipour,Sandro Satta,Mahboobeh Mahmoodi,Argus Sun,Natan Roberto de Barros,Song Li,Tzung K. Hsiai,Nureddin Ashammakhi
出处
期刊:Biofabrication
[IOP Publishing]
日期:2022-04-07
卷期号:15 (2): 022001-022001
被引量:30
标识
DOI:10.1088/1758-5090/ac6538
摘要
Abstract Infectious diseases remain a public healthcare concern worldwide. Amidst the pandemic of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 infection, increasing resources have been diverted to investigate therapeutics targeting the COVID-19 spike glycoprotein and to develop various classes of vaccines. Most of the current investigations employ two-dimensional (2D) cell culture and animal models. However, 2D culture negates the multicellular interactions and three-dimensional (3D) microenvironment, and animal models cannot mimic human physiology because of interspecies differences. On the other hand, organ-on-a-chip (OoC) devices introduce a game-changer to model viral infections in human tissues, facilitating high-throughput screening of antiviral therapeutics. In this context, this review provides an overview of the in vitro OoC-based modeling of viral infection, highlighting the strengths and challenges for the future.
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