Severe asthma: anti-IgE or anti-IL-5?

被引:24
作者
Papathanassiou, Evgenia [1 ]
Loukides, Stelios [1 ]
Bakakos, Petros [2 ]
机构
[1] Univ Athens, Attikon Univ Hosp, Dept Resp Med 2, Athens, Greece
[2] Univ Athens, Dept Resp Med 1, Sotiria Hosp Chest Dis, Sch Med, 11 Kononos Str, GR-11634 Athens, Greece
来源
EUROPEAN CLINICAL RESPIRATORY JOURNAL | 2016年 / 3卷
关键词
severe asthma; monoclonal antibodies; IgE; IL-5; inflammation; asthma control;
D O I
10.3402/ecrj.v3.31813
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Severe asthma is a discrete clinical entity characterised by recurrent exacerbations, reduced quality of life and poor asthma control as ordinary treatment regimens remain inadequate. Difficulty in managing severe asthma derives partly from the multiple existing phenotypes and our inability to recognise them. Though the exact pathogenetic pathway of severe allergic asthma remains unclear, it is known that numerous inflammatory cells and cytokines are involved, and eosinophils represent a key inflammatory cell mediator. Anti-IgE (omalizumab) and anti-IL-5 (mepolizumab) antibodies are biological agents that interfere in different steps of the Th2 inflammatory cascade and are licensed in severe asthma. Both exhibit a favourable clinical outcome as they reduce exacerbation rate and improve asthma control and quality of life, while mepolizumab also induces an oral steroid sparing effect. Nevertheless, it is still questionable which agent is more suitable in the management of severe allergic asthma since no comparable studies have been conducted. Omalizumab's established effectiveness in clinical practice over a long period is complemented by a beneficial effect on airway remodelling process mediated mainly through its impact on eosinophils and other parameters strongly related to eosinophilic inflammation. However, it is possible that mepolizumab through nearly depleting eosinophils could have a similar effect on airway remodelling. Moreover, to date, markers indicative of the patient population responding to each treatment are unavailable although baseline eosinophils and exacerbation rate in the previous year demonstrate a predictive value regarding anti-IL-5 therapy effectiveness. On the other hand, a better therapeutic response for omalizumab has been observed when low forced expiratory volume in 1 sec, high-dose inhaled corticosteroids and increased IgE concentrations are present. Consequently, conclusions are not yet safe to be drawn based on existing knowledge, and additional research is necessary to unravel the remaining issues for the severe asthmatic population.
引用
收藏
页数:9
相关论文
共 73 条
[1]   'Real-life' effectiveness studies of omalizumab in adult patients with severe allergic asthma: systematic review [J].
Abraham, I. ;
Alhossan, A. ;
Lee, C. S. ;
Kutbi, H. ;
MacDonald, K. .
ALLERGY, 2016, 71 (05) :593-610
[2]   Assessing the association between omalizumab and arteriothrombotic events through spontaneous adverse event reporting [J].
Ali, Ayad K. ;
Hartzema, Abraham G. .
JOURNAL OF ASTHMA AND ALLERGY, 2012, 5 :1-9
[3]   Oral Glucocorticoid-Sparing Effect of Mepolizumab in Eosinophilic Asthma [J].
Bel, Elisabeth H. ;
Wenzel, Sally E. ;
Thompson, Philip J. ;
Prazma, Charlene M. ;
Keene, Oliver N. ;
Yancey, Steven W. ;
Ortega, Hector G. ;
Pavord, Ian D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (13) :1189-1197
[4]   Predicting and evaluating response to omalizumab in patients with severe allergic asthma [J].
Bousquet, J. ;
Rabe, K. ;
Humbert, M. ;
Chung, K. F. ;
Berger, W. ;
Fox, H. ;
Ayre, G. ;
Chen, H. ;
Thomas, K. ;
Blogg, M. ;
Holgate, S. .
RESPIRATORY MEDICINE, 2007, 101 (07) :1483-1492
[5]   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
[6]   Predicting response to omalizumab, an anti-IgE antibody, in patients with allergic asthma [J].
Bousquet, J ;
Wenzel, S ;
Holgate, S ;
Lumry, W ;
Freeman, P ;
Fox, H .
CHEST, 2004, 125 (04) :1378-1386
[7]   Asthma - From bronchoconstriction to airways inflammation and remodeling [J].
Bousquet, J ;
Jeffery, PK ;
Busse, WW ;
Johnson, M ;
Vignola, AM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (05) :1720-1745
[8]   EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039
[9]   The eXpeRience registry: The 'real-world' effectiveness of omalizumab in allergic asthma [J].
Braunstahl, G. -J. ;
Chen, C-W ;
Maykut, R. ;
Georgiou, P. ;
Peachey, G. ;
Bruce, J. .
RESPIRATORY MEDICINE, 2013, 107 (08) :1141-1151
[10]   Omalizumab and the risk of malignancy: Results from a pooled analysis [J].
Busse, William ;
Buhl, Roland ;
Vidaurre, Carlos Fernandez ;
Blogg, Martin ;
Zhu, Jin ;
Eisner, Mark D. ;
Canvin, Janice .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (04) :983-U482