Severe Asthma: An Expanding and Mounting Clinical Challenge

被引:32
作者
Bell, Matthew C. [1 ]
Busse, William W. [1 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Sect Allergy Pulm & Crit Care Med, Madison, WI 53792 USA
关键词
Asthma; corticosteroids; bronchodilators; immunomodulators; anti-IgE; SEVERE ALLERGIC-ASTHMA; DOUBLE-BLIND; BRONCHIAL THERMOPLASTY; EOSINOPHILIC ASTHMA; PERSISTENT ASTHMA; CLUSTER-ANALYSIS; OMALIZUMAB; INFLAMMATION; MEPOLIZUMAB; THERAPY;
D O I
10.1016/j.jaip.2013.01.005
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Although all patients with asthma have variable airflow obstruction, airway inflammation, and bronchial hyperresponsiveness, some have disease that is severe in many aspects: persistent airflow obstruction, ongoing symptoms, increased frequency of exacerbations, and, most importantly, a diminished response to medications. A number of definitions have emerged to characterize the clinical features of severe asthma, but a central feature of this phenotype is the need for high doses of medications, especially corticosteroids, in attempts to achieve disease control. The prevalence of severe asthma is also undergoing reevaluation from the usual estimate of 10% to larger numbers on the basis of medication needs and the lack of disease control achieved. At present, the underlying mechanisms of severe asthma are not established but likely reflect a heterogeneous pattern, rather than a single unifying process. Guideline-directed treatment for severe asthma has limits with usual approaches centered on high doses of inhaled corticosteroids, long-acting beta-agonists, and trials with omalizumab, the monoclonal antibody to IgE. With the development of approaches to recognize asthma phenotypes with distinct pathogenesis and hence unique therapeutic targets, it is hoped that a personalized strategy in treatment directed toward disease-specific features will improve outcomes for this high-risk, severely affected population of patients. (C) 2013 American Academy of Allergy, Asthma & Immunology
引用
收藏
页码:110 / 122
页数:13
相关论文
共 58 条
[1]   The ENFUMOSA cross-sectional European multicentre study of the clinical phenotype of chronic severe asthma [J].
Abraham, B ;
Antó, JM ;
Barreiro, E ;
Bel, EHD ;
Bonsignore, G ;
Bousquet, J ;
Castellsague, J ;
Chanez, P ;
Cibella, F ;
Cuttitta, G ;
Dahlén, B ;
Dahlén, SE ;
Drews, N ;
Djukanovic, R ;
Fabbri, LM ;
Folkerts, G ;
Gaga, M ;
Gratziou, C ;
Guerrera, G ;
Holgate, ST ;
Howarth, PH ;
Johnston, SL ;
Kanniess, F ;
Kips, JC ;
Kerstjens, HAM ;
Kumlin, M ;
Magnussen, H ;
Nijkamp, FP ;
Papageorgiou, N ;
Papi, A ;
Postma, DS ;
Pauwels, RA ;
Rabe, KF ;
Richter, K ;
Roldaan, AC ;
Romagnoli, M ;
Roquet, A ;
Sanjuas, C ;
Siafakas, NM ;
Timens, W ;
Tzanakis, N ;
Vachier, I ;
Vignola, AM ;
Watson, L ;
Yourgioti, G .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (03) :470-477
[2]  
Akinbami Lara J, 2012, NCHS Data Brief, P1
[3]  
[Anonymous], 2000, Am J Respir Crit Care Med, V162, P2341
[4]   Global strategy for asthma management and prevention: GINA executive summary [J].
Bateman, E. D. ;
Hurd, S. S. ;
Barnes, P. J. ;
Bousquet, J. ;
Drazen, J. M. ;
FitzGerald, M. ;
Gibson, P. ;
Ohta, K. ;
O'Byrne, P. ;
Pedersen, S. E. ;
Pizzichini, E. ;
Sullivan, S. D. ;
Wenzel, S. E. ;
Zar, H. J. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 31 (01) :143-178
[5]   Can guideline-defined asthma control be achieved? The gaining optimal asthma control study [J].
Bateman, ED ;
Boushey, HA ;
Bousquet, J ;
Busse, WW ;
Clark, TJH ;
Pauwels, RA ;
Pedersen, SE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (08) :836-844
[6]   The effect of treatment with omalizumab, an anti-IgE antibody, on asthma exacerbations and emergency medical visits in patients with severe persistent asthma [J].
Bousquet, J ;
Cabrera, P ;
Berkman, N ;
Buhl, R ;
Holgate, S ;
Wenzel, S ;
Fox, H ;
Hedgecock, S ;
Blogg, M ;
Della Cioppa, G .
ALLERGY, 2005, 60 (03) :302-308
[7]   Uniform definition of asthma severity, control, and exacerbations: Document presented for the World Health Organization Consultation on Severe Asthma [J].
Bousquet, Jean ;
Mantzouranis, Eva ;
Cruz, Alvaro A. ;
Ait-Khaled, Nadia ;
Baena-Cagnani, Carlos E. ;
Bleecker, Eugene R. ;
Brightling, Chris E. ;
Burney, Peter ;
Bush, Andrew ;
Busse, William W. ;
Casale, Thomas B. ;
Chan-Yeung, Moira ;
Chen, Rongchang ;
Chowdhury, Badrul ;
Chung, Kian Fan ;
Dahl, Ronald ;
Drazen, Jeffrey M. ;
Fabbri, Leonardo M. ;
Holgate, Stephen T. ;
Kauffmann, Francine ;
Haahtela, Tari ;
Khaltaev, Nikolai ;
Kiley, James P. ;
Masjedi, Mohammad R. ;
Mohammad, Yousser ;
O'Byrne, Paul ;
Partridge, Martyn R. ;
Rabe, Klaus F. ;
Togias, Alkis ;
van Weel, Christiaan ;
Wenzel, Sally ;
Zhong, Nanshan ;
Zuberbier, Torsten .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 126 (05) :926-938
[8]   Omalizumab, anti-IgE recombinant humanized monoclonal antibody, for the treatment of severe allergic asthma [J].
Busse, W ;
Corren, J ;
Lanier, BQ ;
McAlary, M ;
Fowler-Taylor, A ;
Della Cioppa, G ;
van As, A ;
Gupta, N .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 108 (02) :184-190
[9]   A review of treatment with mepolizumab, an anti-IL-5 mAb, in hypereosinophilic syndromes and asthma [J].
Busse, William W. ;
Ring, Johannes ;
Huss-Marp, Johannes ;
Kahn, Jean-Emmanuel .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 125 (04) :803-813
[10]   Reslizumab for Poorly Controlled, Eosinophilic Asthma A Randomized, Placebo-controlled Study [J].
Castro, Mario ;
Mathur, Sameer ;
Hargreave, Frederick ;
Boulet, Louis-Philippe ;
Xie, Fang ;
Young, James ;
Wilkins, H. Jeffrey ;
Henkel, Timothy ;
Nair, Parameswaran .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 184 (10) :1125-1132