Targeting the IL-33/IL-13 Axis for Respiratory Viral Infections

被引:36
作者
Donovan, Chantal [1 ,2 ]
Bourke, Jane E. [1 ,2 ]
Vlahos, Ross [2 ,3 ]
机构
[1] Monash Univ, Dept Pharmacol, Biomed Discovery Inst, Clayton, Vic 3800, Australia
[2] Univ Melbourne, Lung Hlth Res Ctr, Dept Pharmacol & Therapeut, Melbourne, Vic 3010, Australia
[3] RMIT Univ, Sch Hlth & Biomed Sci, Melbourne, Vic, Australia
关键词
INDUCED AIRWAY HYPERRESPONSIVENESS; INFLUENZA-VIRUS INFECTION; GOBLET CELL HYPERPLASIA; INNATE LYMPHOID-CELLS; CIGARETTE-SMOKE; EPITHELIAL-CELLS; ASTHMA EXACERBATIONS; DENDRITIC CELLS; GUINEA-PIG; IL-33;
D O I
10.1016/j.tips.2016.01.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lung diseases, such as asthma and chronic obstructive pulmonary disease (COPD), are highly prevalent worldwide. One of the major factors that limits the efficacy of current medication in these patients are viral infections, leading to exacerbations of symptoms and decreased quality of life. Current pharmacological strategies targeting virus-induced lung disease are problematic due to antiviral resistance and the requirement for strain-specific vaccination. Thus, new therapeutic strategies are urgently required. In this Opinion article, we provide state-of-the-art evidence from humans and preclinical animal models implicating the interleukin (IL)-33/IL-13 axis in virus-induced lung disease. Thus, targeting the IL-33/IL-13 axis may be a feasible way to overcome the limitations of current therapy used to treat virus-induced exacerbations of lung disease.
引用
收藏
页码:252 / 261
页数:10
相关论文
共 98 条
[91]   Critical role for IL-13 in the development of allergen-induced airway hyperreactivity [J].
Walter, DM ;
McIntire, JJ ;
Berry, G ;
McKenzie, ANJ ;
Donaldson, DD ;
DeKruyff, RH ;
Umetsu, DT .
JOURNAL OF IMMUNOLOGY, 2001, 167 (08) :4668-4675
[92]   Inhibition of T1/ST2 during respiratory syncytial virus infection prevents T helper cell type 2 (Th2)- but not Th1-driven immunopathology [J].
Walzl, G ;
Matthews, S ;
Kendall, S ;
Gutierrez-Ramos, JC ;
Coyle, AJ ;
Openshaw, PJM ;
Hussell, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (07) :785-792
[93]   Asthmatic bronchial epithelial cells have a deficient innate immune response to infection with rhinovirus [J].
Wark, PAB ;
Johnston, SL ;
Bucchieri, F ;
Powell, R ;
Puddicombe, S ;
Laza-Stanca, V ;
Holgate, ST ;
Davies, DE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (06) :937-947
[94]   Viral and bacterial infection in acute asthma and chronic obstructive pulmonary disease increases the risk of readmission [J].
Wark, Peter A. B. ;
Tooze, Melinda ;
Powell, Heather ;
Parsons, Kristy .
RESPIROLOGY, 2013, 18 (06) :996-1002
[95]   Interleukin-13: Central mediator of allergic asthma [J].
Wills-Karp, M ;
Luyimbazi, J ;
Xu, XY ;
Schofield, B ;
Neben, TY ;
Karp, CL ;
Donaldson, DD .
SCIENCE, 1998, 282 (5397) :2258-2261
[96]   Over-expression of IL-33 leads to spontaneous pulmonary inflammation in mIL-33 transgenic mice [J].
Xiang, Zhiguang ;
Chen, Wei ;
Ravary, Steven ;
Dong, Wei ;
Zhang, Wei ;
Mu, Rong ;
Li, Zhanguo ;
Zhang, Lianfeng .
IMMUNOLOGY LETTERS, 2010, 131 (02) :159-165
[97]   Role of Nrf2 in Host Defense against Influenza Virus in Cigarette Smoke-Exposed Mice [J].
Yageta, Yuichi ;
Ishii, Yukio ;
Morishima, Yuko ;
Masuko, Hironori ;
Ano, Satoshi ;
Yamadori, Tadahiro ;
Itoh, Ken ;
Takeuchi, Kaoru ;
Yamamoto, Masayuki ;
Hizawa, Nobuyuki .
JOURNAL OF VIROLOGY, 2011, 85 (10) :4679-4690
[98]   Interleukin-13 mediates airways hyperreactivity through the IL-4 receptor-alpha chain and STAT-6 independently of IL-5 and eotaxin [J].
Yang, M ;
Hogan, SP ;
Henry, PJ ;
Matthaei, KI ;
McKenzie, ANJ ;
Young, IG ;
Rothenberg, ME ;
Foster, PS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 25 (04) :522-530