Animal Models of Allergic Airways Disease: Where Are We and Where to Next?

被引:47
作者
Chapman, David G. [1 ,2 ]
Tully, Jane E. [3 ]
Nolin, James D. [3 ]
Janssen-Heininger, Yvonne M. [3 ]
Irvin, Charles G. [1 ]
机构
[1] Univ Vermont, Coll Med, Dept Med, Burlington, VT 05405 USA
[2] Univ Sydney, Sydney Med Sch, Woolcock Inst Med Res, Sydney, NSW 2006, Australia
[3] Univ Vermont, Coll Med, Dept Pathol, Burlington, VT 05405 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
ASTHMA; AIRWAY HYPERRESPONSIVENESS; ANIMAL MODELS; HOUSE-DUST MITE; KAPPA-B ACTIVATION; CLUSTER-ANALYSIS; ASTHMA RESEARCH; OZONE EXPOSURE; MOUSE MODEL; INFLAMMATION; HYPERRESPONSIVENESS; MICE; OBESITY;
D O I
10.1002/jcb.24881
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In a complex inflammatory airways disease such as asthma, abnormalities in a plethora of molecular and cellular pathways ultimately culminate in characteristic impairments in respiratory function. The ability to study disease pathophysiology in the setting of a functioning immune and respiratory system therefore makes mouse models an invaluable tool in translational research. Despite the vast understanding of inflammatory airways diseases gained from mouse models to date, concern over the validity of mouse models continues to grow. Therefore the aim of this review is twofold; firstly, to evaluate mouse models of asthma in light of current clinical definitions, and secondly, to provide a framework by which mouse models can be continually refined so that they continue to stand at the forefront of translational science. Indeed, it is in viewing mouse models as a continual work in progress that we will be able to target our research to those patient populations in whom current therapies are insufficient. J. Cell. Biochem. 115: 2055-2064, 2014. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:2055 / 2064
页数:10
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