Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, CB3 0AS, UK.
Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, CB2 0AW, UK.
Adv Sci (Weinh). 2024 Feb;11(8):e2306727. doi: 10.1002/advs.202306727. Epub 2023 Dec 28.
Infectious diseases are increasingly recognized as a major threat worldwide due to the rise of antimicrobial resistance and the emergence of novel pathogens. In vitro models that can adequately mimic in vivo gastrointestinal physiology are in high demand to elucidate mechanisms behind pathogen infectivity, and to aid the design of effective preventive and therapeutic interventions. There exists a trade-off between simple and high throughput models and those that are more complex and physiologically relevant. The complexity of the model used shall be guided by the biological question to be addressed. This review provides an overview of the structure and function of the intestine and the models that are developed to emulate this. Conventional models are discussed in addition to emerging models which employ engineering principles to equip them with necessary advanced monitoring capabilities for intestinal host-pathogen interrogation. Limitations of current models and future perspectives on the field are presented.
传染病由于抗微生物药物耐药性的出现和新病原体的出现,日益被认为是全世界的一个主要威胁。人们迫切需要能够充分模拟体内胃肠道生理学的体外模型,以阐明病原体感染背后的机制,并帮助设计有效的预防和治疗干预措施。简单和高通量的模型与更复杂和更具生理相关性的模型之间存在着权衡。模型的复杂性应根据要解决的生物学问题来指导。本综述概述了肠道的结构和功能,以及为模拟肠道而开发的模型。除了新兴的模型外,本文还讨论了传统模型,这些新兴模型采用了工程原理为其配备了对肠道宿主-病原体研究所需的必要先进监测能力。本文还介绍了当前模型的局限性和该领域的未来展望。