Moving towards a new generation of animal models for asthma and COPD with improved clinical relevance

被引:87
作者
Stevenson, Christopher S. [1 ,2 ,3 ,4 ]
Birrell, Mark A. [2 ,3 ,4 ]
机构
[1] Hoffmann La Roche, Inflammat Discovery, Inflammat Discovery Translat Area, Nutley, NJ 07110 USA
[2] Imperial Coll Sch Med, Resp Pharmacol Pharmacol & Toxicol Sect, Natl Heart & Lung Inst, London, England
[3] Imperial Coll Sch Med, Ctr Integrat Mammalian Physiol & Pharmacol, London, England
[4] Imperial Coll Sch Med, Ctr Resp Infect, London, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Asthma; COPD; Airway inflammation; Acute exacerbation; Airway remodeling; Emphysema; RESPIRATORY-SYNCYTIAL-VIRUS; OBSTRUCTIVE PULMONARY-DISEASE; HOUSE-DUST MITE; SMOKE-INDUCED EMPHYSEMA; ALLERGIC LUNG INFLAMMATION; ELASTASE-INDUCED EMPHYSEMA; COLONY-STIMULATING FACTOR; CHRONIC AIRWAY INFLAMMATION; RETINOIC ACID RECEPTORS; NECROSIS-FACTOR-ALPHA;
D O I
10.1016/j.pharmthera.2010.10.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Asthma and chronic obstructive pulmonary disease (COPD) are complex inflammatory airway diseases characterised by airflow obstruction that remain leading causes of hospitalization and death worldwide. Animal modelling systems that accurately reflect disease pathophysiology continue to be essential to the development of new therapies for both conditions. In this review, we describe preclinical in vivo models that recapitulate many of the features of asthma and COPD. Specifically, we discuss the pro's and con's of the standard models and highlight recently developed systems designed to more accurately reflect the complexity of both diseases. For instance, clinically relevant allergens (i.e. house dust mite) are now being used to mimic the inflammatory changes and airway remodelling that result after chronic allergen exposures. Additionally, systems are being developed to mimic steroid-resistant and viral exacerbations of allergic inflammation - aspects of asthma where there is an acute need for new therapies. Similarly, COPD models have evolved to align with the improved clinical understanding of the factors contributing to disease progression. This includes using cigarette smoke to model not only airway inflammation and remodelling, but some systemic changes (e.g. hypertension and skeletal muscle alterations) that are thought to influence disease. Further, mouse genetics are being exploited to gain insights into the genetics of COPD susceptibility. The new models of asthma and COPD described herein demonstrate that improved clinical understanding of the diseases and better preclinical models is an iterative process that will hopefully lead to therapies that can effectively manage severe asthma and COPD. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 105
页数:13
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