Wang Yaqing, Wang Peng, Qin Jianhua
Division of Biotechnology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing, China.
Acc Chem Res. 2021 Sep 21;54(18):3550-3562. doi: 10.1021/acs.accounts.1c00411. Epub 2021 Aug 29.
Infectious diseases present tremendous challenges to human progress and public health. The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the associated coronavirus disease 2019 (COVID-19) pandemic continue to pose an imminent threat to humanity. These infectious diseases highlight the importance of developing innovative strategies to study disease pathogenesis and protect human health. Although conventional cell culture and animal models are useful in facilitating the development of effective therapeutics for infectious diseases, models that can accurately reflect human physiology and human-relevant responses to pathogens are still lacking. Microfluidic organs-on-a-chip (organ chips) are engineered microfluidic cell culture devices lined with living cells, which can resemble organ-level physiology with high fidelity by rebuilding tissue-tissue interfaces, mechanical cues, fluidic flow, and the biochemical cellular microenvironment. They present a unique opportunity to bridge the gap between experimental models and human pathophysiology and are thus a promising platform for disease studies and drug testing. In this Account, we first introduce how recent progress in organ chips has enabled the recreation of complex pathophysiological features of human infections . Next, we describe the progress made by our group in adopting organ chips and other microphysiological systems for the study of infectious diseases, including SARS-CoV-2 viral infections and intrauterine bacterial infections. Respiratory symptoms dominate the clinical manifestations of many COVID-19 patients, even involving the systemic injury of many distinct organs, such as the lung, the gastrointestinal tract, and so forth. We thus particularly highlight our recent efforts to explore how lung-on-a-chip and intestine-on-a-chip might be useful in addressing the ongoing viral pandemic of COVID-19 caused by SARS-CoV-2. These organ chips offer a potential platform for studying virus-host interactions and human-relevant responses as well as accelerating the development of effective therapeutics against COVID-19. Finally, we discuss opportunities and challenges in the development of next-generation organ chips, which are urgently needed for developing effective and affordable therapies to combat infectious diseases. We hope that this Account will promote awareness about organ microphysiological systems for modeling infections and stimulate joint efforts across multiple disciplines to understand emerging and re-emerging pandemic diseases and rapidly identify innovative interventions.
传染病对人类发展和公共卫生构成了巨大挑战。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的出现以及相关的2019冠状病毒病(COVID-19)大流行继续对人类构成紧迫威胁。这些传染病凸显了制定创新策略来研究疾病发病机制和保护人类健康的重要性。尽管传统的细胞培养和动物模型有助于开发针对传染病的有效疗法,但仍缺乏能够准确反映人类生理学以及人类对病原体相关反应的模型。微流控器官芯片是一种由活细胞排列的工程化微流控细胞培养装置,通过重建组织-组织界面、机械信号、流体流动和生化细胞微环境,能够高度逼真地模拟器官水平的生理学。它们为弥合实验模型与人类病理生理学之间的差距提供了独特的机会,因此是疾病研究和药物测试的一个有前景的平台。在本综述中,我们首先介绍器官芯片的最新进展如何实现了人类感染复杂病理生理特征的重现。接下来,我们描述我们团队在采用器官芯片和其他微生理系统研究传染病方面所取得的进展,包括SARS-CoV-2病毒感染和宫内细菌感染。呼吸道症状在许多COVID-19患者的临床表现中占主导地位,甚至涉及许多不同器官的全身性损伤,如肺、胃肠道等。因此,我们特别强调我们最近为探索芯片肺和芯片肠道如何有助于应对由SARS-CoV-2引起的当前COVID-19病毒大流行所做的努力。这些器官芯片为研究病毒-宿主相互作用和人类相关反应以及加速针对COVID-19的有效疗法的开发提供了一个潜在平台。最后,我们讨论了下一代器官芯片开发中的机遇和挑战,这对于开发有效且经济实惠的传染病治疗方法来说是迫切需要的。我们希望本综述将提高人们对用于模拟感染的器官微生理系统的认识,并激发多学科的共同努力,以了解新出现和再次出现的大流行疾病,并迅速确定创新的干预措施。