Division of Cardiology and Department of Bioengineering, School of Engineering (S.S., K.W., S.W., T.K.H.), University of California, Los Angeles.
Division of Cardiology, Department of Medicine, School of Medicine (S.S., K.W., S.W., T.K.H.), University of California, Los Angeles.
Circ Res. 2023 May 12;132(10):1405-1424. doi: 10.1161/CIRCRESAHA.122.321877. Epub 2023 May 11.
SARS-CoV-2, the virus underlying COVID-19, has now been recognized to cause multiorgan disease with a systemic effect on the host. To effectively combat SARS-CoV-2 and the subsequent development of COVID-19, it is critical to detect, monitor, and model viral pathogenesis. In this review, we discuss recent advancements in microfluidics, organ-on-a-chip, and human stem cell-derived models to study SARS-CoV-2 infection in the physiological organ microenvironment, together with their limitations. Microfluidic-based detection methods have greatly enhanced the rapidity, accessibility, and sensitivity of viral detection from patient samples. Engineered organ-on-a-chip models that recapitulate in vivo physiology have been developed for many organ systems to study viral pathology. Human stem cell-derived models have been utilized not only to model viral tropism and pathogenesis in a physiologically relevant context but also to screen for effective therapeutic compounds. The combination of all these platforms, along with future advancements, may aid to identify potential targets and develop novel strategies to counteract COVID-19 pathogenesis.
SARS-CoV-2,即引发 COVID-19 的病毒,现已被证实可导致多器官疾病,并对宿主产生全身性影响。为了有效对抗 SARS-CoV-2 及其引发的 COVID-19,检测、监测和模拟病毒发病机制至关重要。在这篇综述中,我们讨论了微流控、类器官芯片和人类干细胞衍生模型在研究 SARS-CoV-2 感染生理器官微环境方面的最新进展,以及它们的局限性。基于微流控的检测方法极大地提高了从患者样本中快速、便捷、灵敏地检测病毒的能力。已经开发出了许多用于模拟体内生理学的工程类器官芯片模型,用于研究病毒病理学。人类干细胞衍生模型不仅可用于在生理相关环境中模拟病毒嗜性和发病机制,还可用于筛选有效的治疗化合物。所有这些平台的结合,以及未来的进展,可能有助于确定潜在的靶点,并开发新的策略来对抗 COVID-19 的发病机制。