Anti-IgE treatment, airway inflammation and remodelling in severe allergic asthma: current knowledge and future perspectives

被引:109
作者
Samitas, Konstantinos [1 ,2 ]
Delimpoura, Vasiliki [1 ]
Zervas, Eleftherios [1 ]
Gaga, Mina [1 ]
机构
[1] Athens Chest Hosp Sotiria, Resp Dept & Asthma Ctr 7, Athens 11527, Greece
[2] Acad Athens, Biomed Res Fdn, Ctr Basic Res, Div Cell Biol,Cellular Immunol Lab, Athens, Greece
关键词
D O I
10.1183/16000617.00001715
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Asthma is a disorder of the airways involving various inflammatory cells and mediators and characterised by bronchial hyperresponsiveness, chronic inflammation and structural alterations in the airways, also known as remodelling. IgE is an important mediator of allergic reactions and has a central role in allergic asthma pathophysiology, as it is implicated in both the early and late phase allergic response. Moreover, clinical and mechanistic evidence has lately emerged, implicating IgE in the development of airway remodelling. The use of monoclonal antibodies targeting IgE, such as omalizumab, has proven very effective in improving respiratory symptoms and quality of life, while reducing asthma exacerbations, emergency room visits and the use of systemic corticosteroids in allergic severe asthma. These effects are believed to be mainly mediated by omalizumab's inhibitory effect on the initiation and further propagation of the allergic inflammation cascade. However, there is evidence to suggest that anti-IgE treatment remains effective long after it has been discontinued. In part, these findings could be attributed to the possible ameliorating effects of anti-IgE treatment on airway remodelling. In this review, we discuss recent findings supporting the notion that anti- IgE treatment modulates the complex immune responses that manifest clinically as asthma and ameliorates airway remodelling changes often observed in allergic severe asthma phenotypes.
引用
收藏
页码:594 / 601
页数:8
相关论文
共 75 条
[1]
Pharmacokinetics, pharmacodynamics and safety of QGE031 (ligelizumab), a novel high-affinity anti-IgE antibody, in atopic subjects [J].
Arm, J. P. ;
Bottoli, I. ;
Skerjanec, A. ;
Floch, D. ;
Groenewegen, A. ;
Maahs, S. ;
Owen, C. E. ;
Jones, I. ;
Lowe, P. J. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2014, 44 (11) :1371-1385
[2]
Bronchoalveolar lavage fluid concentrations of transforming growth factor (TGF)-β1, TGF-β2, interleukin (IL)-4 and IL-13 after segmental allergen challenge and their effects on α-smooth muscle actin and collagen III synthesis by primary human lung fibroblasts [J].
Batra, V ;
Musani, AI ;
Hastie, AT ;
Khurana, S ;
Carpenter, KA ;
Zangrilli, JG ;
Peters, SP .
CLINICAL AND EXPERIMENTAL ALLERGY, 2004, 34 (03) :437-444
[3]
"Real-life" effectiveness of omalizumab in patients with severe persistent allergic asthma: The PERSIST study [J].
Brusselle, G. ;
Michils, A. ;
Louis, R. ;
Dupont, L. ;
de Maele, B. Van ;
Delobbe, A. ;
Pilette, C. ;
Lee, C. S. ;
Gurdain, S. ;
Vancayzeele, S. ;
Lecomte, P. ;
Hermans, C. ;
MacDonald, K. ;
Song, M. ;
Abraham, I. .
RESPIRATORY MEDICINE, 2009, 103 (11) :1633-1642
[4]
Anti-IgE: lessons from clinical trials in patients with severe allergic asthma symptomatic despite optimised therapy [J].
Buhl, R. .
EUROPEAN RESPIRATORY REVIEW, 2007, 16 (104) :73-77
[5]
Expression of the high-affinity receptor for IgE on bronchial epithelial cells of asthmatics [J].
Campbell, AM ;
Vachier, I ;
Chanez, P ;
Vignola, AM ;
Label, B ;
Kochan, J ;
Godard, P ;
Bousquet, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (01) :92-97
[6]
Chan Marcia A, 2013, Clin Transl Allergy, V3, P29, DOI 10.1186/2045-7022-3-29
[7]
Omalizumab-induced decrease of FcεRI expression in patients with severe allergic asthma [J].
Chanez, Pascal ;
Contin-Bordes, Cecile ;
Garcia, Gilles ;
Verkindre, Christophe ;
Didier, Alain ;
De Blay, Frederic ;
de Lara, Manuel Tunon ;
Blanco, Patrick ;
Moreau, Jean-Francois ;
Robinson, Philip ;
Bourdeix, Isabelle ;
Trunet, Patrick ;
Le Gros, Vincent ;
Humbert, Marc ;
Molimard, Mathieu .
RESPIRATORY MEDICINE, 2010, 104 (11) :1608-1617
[8]
Anti-IgE antibodies for the treatment of IgE-mediated allergic diseases [J].
Chang, Tse Wen ;
Wu, Pheidias C. ;
Hsu, C. Long ;
Hung, Alfur F. .
ADVANCES IN IMMUNOLOGY, VOL 93, 2007, 93 :63-119
[9]
The pharmacological basis of anti-IgE therapy [J].
Chang, TW .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :157-162
[10]
Anti-IgE as a mast cell-stabilizing therapeutic agent [J].
Chang, TW ;
Shiung, YY .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (06) :1203-1212