The role of viruses in acute exacerbations of asthma

被引:287
作者
Jackson, David J. [1 ]
Johnston, Sebastian L. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Resp Med, Natl Heart & Lung Inst, London W2 1PG, England
基金
英国医学研究理事会;
关键词
Asthma; acute exacerbation; virus; RESPIRATORY SYNCYTIAL VIRUS; NF-KAPPA-B; INTERCELLULAR-ADHESION MOLECULE-1; BRONCHIAL EPITHELIAL-CELLS; RHINOVIRUS; 16; INFECTION; ENDOTHELIAL GROWTH-FACTOR; MESSENGER-RNA EXPRESSION; TOLL-LIKE RECEPTOR-3; ANTIVIRAL ACTIVITY; IN-VITRO;
D O I
10.1016/j.jaci.2010.04.021
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Viral respiratory infections are the most common cause of an acute asthma exacerbation in both children and adults and represent a significant global health burden. An increasing body of evidence supports the hypothesis that these infections cause a greater degree of morbidity in asthmatic subjects than in the healthy population, emphasizing a discrepancy in the antiviral response of asthmatics. In this review we discuss why such a discrepancy might exist, examining the role of the bronchial epithelium as well as the main inflammatory cells, mediators, and molecular pathways that are involved in the immune response. In addition, the potential impact of virus-induced asthma exacerbations on airway remodelling is reviewed and we explore which therapeutic options might be of benefit in preventing the deterioration of asthma control seen following viral infection. (J Allergy Clin Immunol 2010;125:1178-87.)
引用
收藏
页码:1178 / 1187
页数:10
相关论文
共 129 条
[1]   PATHOLOGICAL CHANGES IN VIRUS INFECTIONS OF LOWER RESPIRATORY TRACT IN CHILDREN [J].
AHERNE, W ;
BIRD, T ;
COURT, SDM ;
GARDNER, PS ;
MCQUILLIN, J .
JOURNAL OF CLINICAL PATHOLOGY, 1970, 23 (01) :7-+
[2]   Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3 [J].
Alexopoulou, L ;
Holt, AC ;
Medzhitov, R ;
Flavell, RA .
NATURE, 2001, 413 (6857) :732-738
[3]   DETECTION OF RHINOVIRUS INFECTION OF THE NASAL-MUCOSA BY OLIGONUCLEOTIDE IN-SITU HYBRIDIZATION [J].
BARDIN, PG ;
JOHNSTON, SL ;
SANDERSON, G ;
ROBINSON, BS ;
PICKETT, MA ;
FRAENKEL, DJ ;
HOLGATE, ST .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (02) :207-213
[4]   Mouse models of rhinovirus-induced disease and exacerbation of allergic airway inflammation [J].
Bartlett, Nathan W. ;
Walton, Ross P. ;
Edwards, Michael R. ;
Aniscenko, Juliya ;
Caramori, Gaetano ;
Zhu, Jie ;
Glanville, Nicholas ;
Choy, Katherine J. ;
Jourdan, Patrick ;
Burnet, Jerome ;
Tuthill, Tobias J. ;
Pedrick, Michael S. ;
Hurle, Michael J. ;
Plumpton, Chris ;
Sharp, Nigel A. ;
Bussell, James N. ;
Swallow, Dallas M. ;
Schwarze, Jurgen ;
Guy, Bruno ;
WAlmond, Jeffrey ;
Jeffery, Peter K. ;
Lloyd, Clare M. ;
Papi, Alberto ;
Killington, Richard A. ;
Rowlands, David J. ;
Blair, Edward D. ;
Clarke, Neil J. ;
Johnston, Sebastian L. .
NATURE MEDICINE, 2008, 14 (02) :199-204
[5]   Contribution of Bronchial Fibroblasts to the Antiviral Response in Asthma [J].
Bedke, Nicole ;
Haitchi, Hans Michael ;
Xatzipsalti, Mara ;
Holgate, Stephen T. ;
Davies, Donna E. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (06) :3660-3667
[6]   Conservation of amino acids in human rhinovirus 3C protease correlates with broad-spectrum antiviral activity of rupintrivir, a novel human rhinovirus 3C protease inhibitor [J].
Binford, SL ;
Maldonado, F ;
Brothers, MA ;
Weady, PT ;
Zalman, LS ;
Meador, JW ;
Matthews, DA ;
Patick, AK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :619-626
[7]   Rhinovirus-induced modulation of gene expression in bronchial epithelial cells from subjects with asthma [J].
Bochkov, Y. A. ;
Hanson, K. M. ;
Keles, S. ;
Brockman-Schneider, R. A. ;
Jarjour, N. N. ;
Gern, J. E. .
MUCOSAL IMMUNOLOGY, 2010, 3 (01) :69-80
[8]   Type III IFN-λ mRNA expression in sputum of adult and school-aged asthmatics [J].
Bullens, Dominique M. A. ;
Decraene, A. ;
Dilissen, E. ;
Meyts, I. ;
De Boeck, K. ;
Dupont, L. J. ;
Ceuppens, J. L. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2008, 38 (09) :1459-1467
[9]   A COMMON COLD VIRUS, RHINOVIRUS-16, POTENTIATES AIRWAY INFLAMMATION AFTER SEGMENTAL ANTIGEN BRONCHOPROVOCATION IN ALLERGIC SUBJECTS [J].
CALHOUN, WJ ;
DICK, EC ;
SCHWARTZ, LB ;
BUSSE, WW .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2200-2208
[10]  
CARBONELLESTRAN.X, 2007, PED AM SOC ANN M MAY