Yaqub Naheem, Wayne Gareth, Birchall Martin, Song Wenhui
UCL Centre for Biomaterials in Surgical Reconstruction and Regeneration, Department of Surgical Biotechnology, Division of Surgery & Interventional Science, University College London, London NW3 2PF, UK.
Novel Human Genetics, GlaxoSmithKline, Stevenage SG1 2NY, UK.
Biotechnol Adv. 2022 Jan-Feb;54:107832. doi: 10.1016/j.biotechadv.2021.107832. Epub 2021 Sep 2.
The respiratory epithelium is intimately associated with the pathophysiologies of highly infectious viral contagions and chronic illnesses such as chronic obstructive pulmonary disorder, presently the third leading cause of death worldwide with a projected economic burden of £1.7 trillion by 2030. Preclinical studies of respiratory physiology have almost exclusively utilised non-humanised animal models, alongside reductionistic cell line-based models, and primary epithelial cell models cultured at an air-liquid interface (ALI). Despite their utility, these model systems have been limited by their poor correlation to the human condition. This has undermined the ability to identify novel therapeutics, evidenced by a 15% chance of success for medicinal respiratory compounds entering clinical trials in 2018. Consequently, preclinical studies require new translational efficacy models to address the problem of respiratory drug attrition. This review describes the utility of the current in vivo (rodent), ex vivo (isolated perfused lungs and precision cut lung slices), two-dimensional in vitro cell-line (A549, BEAS-2B, Calu-3) and three-dimensional in vitro ALI (gold-standard and co-culture) and organoid respiratory epithelium models. The limitations to the application of these model systems in drug discovery research are discussed, in addition to perspectives of the future innovations required to facilitate the next generation of human-relevant respiratory models.
呼吸道上皮与高传染性病毒感染以及慢性疾病(如慢性阻塞性肺疾病,目前是全球第三大死因,预计到2030年经济负担将达1.7万亿英镑)的病理生理学密切相关。呼吸道生理学的临床前研究几乎完全使用非人源化动物模型,以及基于细胞系的简化模型和在气液界面(ALI)培养的原代上皮细胞模型。尽管这些模型系统有其用途,但它们与人类状况的相关性较差,受到了限制。这削弱了识别新型治疗方法的能力,2018年进入临床试验的药用呼吸化合物成功的几率为15%就证明了这一点。因此,临床前研究需要新的转化效能模型来解决呼吸药物损耗的问题。本综述描述了当前体内(啮齿动物)、体外(离体灌注肺和精密切割肺切片)、二维体外细胞系(A549、BEAS-2B、Calu-3)以及三维体外ALI(金标准和共培养)和类器官呼吸道上皮模型的效用。除了对促进下一代与人类相关的呼吸道模型所需的未来创新的展望外,还讨论了这些模型系统在药物发现研究中的应用局限性。