Saygili Ecem, Yildiz-Ozturk Ece, Green Macauley J, Ghaemmaghami Amir M, Yesil-Celiktas Ozlem
Department of Bioengineering, Faculty of Engineering, Ege University, 35100 Izmir, Turkey.
Translational Pulmonary Research Center, Ege University, 35100 Izmir, Turkey.
Biomicrofluidics. 2021 Mar 23;15(2):021501. doi: 10.1063/5.0038924. eCollection 2021 Mar.
Respiratory viral infections are leading causes of death worldwide. A number of human respiratory viruses circulate in all age groups and adapt to person-to-person transmission. It is vital to understand how these viruses infect the host and how the host responds to prevent infection and onset of disease. Although animal models have been widely used to study disease states, incisive arguments related to poor prediction of patient responses have led to the development of microfluidic organ-on-chip models, which aim to recapitulate organ-level physiology. Over the past decade, human lung chips have been shown to mimic many aspects of the lung function and its complex microenvironment. In this review, we address immunological responses to viral infections and elaborate on human lung airway and alveolus chips reported to model respiratory viral infections and therapeutic interventions. Advances in the field will expedite the development of therapeutics and vaccines for human welfare.
呼吸道病毒感染是全球主要死因。多种人类呼吸道病毒在所有年龄组中传播,并适应人际传播。了解这些病毒如何感染宿主以及宿主如何做出反应以预防感染和疾病发作至关重要。尽管动物模型已被广泛用于研究疾病状态,但与患者反应预测不佳相关的尖锐争议促使了微流控芯片器官模型的发展,该模型旨在重现器官水平的生理学。在过去十年中,人类肺芯片已被证明能够模拟肺功能及其复杂微环境的许多方面。在这篇综述中,我们阐述了对病毒感染的免疫反应,并详细介绍了据报道用于模拟呼吸道病毒感染和治疗干预的人类肺气道和肺泡芯片。该领域的进展将加速用于人类福祉的治疗方法和疫苗的开发。