Duncan Gregg A, Jung James, Hanes Justin, Suk Jung Soo
Center for Nanomedicine, Johns Hopkins University, Baltimore, Maryland, USA.
Department of Ophthalmology, Johns Hopkins University, Baltimore, Maryland, USA.
Mol Ther. 2016 Dec;24(12):2043-2053. doi: 10.1038/mt.2016.182. Epub 2016 Sep 20.
Recent evidence suggests that the airway mucus gel layer may be impermeable to the viral and synthetic gene vectors used in past inhaled gene therapy clinical trials for diseases like cystic fibrosis. These findings support the logic that inhaled gene vectors that are incapable of penetrating the mucus barrier are unlikely to provide meaningful benefit to patients. In this review, we discuss the biochemical and biophysical features of mucus that contribute its barrier function, and how these barrier properties may be reinforced in patients with lung disease. We next review biophysical techniques used to assess the potential ability of gene vectors to penetrate airway mucus. Finally, we provide new data suggesting that fresh human airway mucus should be used to test the penetration rates of gene vectors. The physiological barrier properties of spontaneously expectorated CF sputum remained intact up to 24 hours after collection when refrigerated at 4 °C. Conversely, the barrier properties were significantly altered after freezing and thawing of sputum samples. Gene vectors capable of overcoming the airway mucus barrier hold promise as a means to provide the widespread gene transfer throughout the airway epithelium required to achieve meaningful patient outcomes in inhaled gene therapy clinical trials.
最近的证据表明,气道黏液凝胶层可能会阻碍过去用于囊性纤维化等疾病吸入式基因治疗临床试验中的病毒和合成基因载体。这些发现支持了这样一种逻辑,即无法穿透黏液屏障的吸入式基因载体不太可能给患者带来显著益处。在这篇综述中,我们讨论了黏液的生化和生物物理特性如何促成其屏障功能,以及这些屏障特性在肺病患者中可能如何增强。接下来,我们回顾了用于评估基因载体穿透气道黏液潜在能力的生物物理技术。最后,我们提供了新的数据,表明应使用新鲜的人气道黏液来测试基因载体的穿透率。收集后在4°C冷藏时,自发性咳出的囊性纤维化痰液的生理屏障特性在长达24小时内保持完整。相反,痰液样本冷冻和解冻后,其屏障特性会发生显著改变。能够克服气道黏液屏障的基因载体有望作为一种手段,在吸入式基因治疗临床试验中实现有意义的患者治疗效果所需的整个气道上皮的广泛基因转移。