Allen Irving C
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Methods Mol Biol. 2013;1032:159-72. doi: 10.1007/978-1-62703-496-8_13.
Mouse models of allergic airway inflammation have proven essential in understanding the mechanisms and pathophysiology underling human asthma. There is a diverse range of mouse models described in the literature that typically vary slightly by allergen, duration of exposure, and route of sensitization. In general, each of these models has proven to be acceptable surrogates for studying specific aspects of the human disease, including airway inflammation, airway hyperresponsiveness (AHR), and airway remodeling. Here, we describe a highly versatile model based on nasal sensitization with house dust mite antigen (DMA). Mice receive multiple intranasal inoculations with DMA each week for a period of 4-16 weeks, which results in increased Th2-mediated airway inflammation and AHR. However, an added feature of the long--term exposures described here is the ability to more accurately evaluate the impact of chronic inflammation on airway remodeling and lung pathophysiology in response to a clinically relevant allergen.
事实证明,过敏性气道炎症的小鼠模型对于理解人类哮喘的发病机制和病理生理学至关重要。文献中描述了各种各样的小鼠模型,这些模型通常在过敏原、暴露持续时间和致敏途径上略有不同。一般来说,这些模型中的每一种都已被证明是研究人类疾病特定方面的可接受替代模型,包括气道炎症、气道高反应性(AHR)和气道重塑。在此,我们描述一种基于用屋尘螨抗原(DMA)进行鼻腔致敏的高度通用的模型。小鼠每周接受多次DMA鼻内接种,持续4至16周,这会导致Th2介导的气道炎症和AHR增加。然而,此处描述的长期暴露的一个附加特点是能够更准确地评估慢性炎症对气道重塑和肺病理生理学的影响,以应对临床相关过敏原。