The Complex Type 2 Endotype in Allergy and Asthma: From Laboratory to Bedside

被引:71
作者
Agache, Ioana [1 ]
Sugita, Kazunari [2 ,3 ]
Morita, Hideaki [2 ,3 ]
Akdis, Muebeccel [2 ,3 ]
Akdis, Cezmi A. [2 ,3 ]
机构
[1] Transylvania Univ Brasov, Fac Med, Dept Allergy & Clin Immunol, Brasov, Romania
[2] Univ Zurich, Swiss Inst Allergy & Asthma Res SIAF, Davos, Switzerland
[3] CKCARE, Davos, Switzerland
关键词
Allergy; Phenotype; Endotype; Th2; inflammation; Asthma; Rhinitis; INNATE LYMPHOID-CELLS; THYMIC STROMAL LYMPHOPOIETIN; EXHALED NITRIC-OXIDE; CRTH2 ANTAGONIST OC000459; CHRONIC RHINOSINUSITIS; NASAL POLYPS; IFN-GAMMA; AIRWAY INFLAMMATION; EOSINOPHIL COUNTS; ATOPIC-DERMATITIS;
D O I
10.1007/s11882-015-0529-x
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Better management of allergic diseases needs a sharpened understanding of disease heterogeneity and mechanisms in relation to clinically significant outcomes. Phenotypes describing observable clinical and morphologic characteristics and unique responses to treatment have been developed; however, they do not relate to disease mechanisms. Recently, extended heterogeneous and disease-related metabolic, inflammatory, immunological, and remodeling pathways have been described, and reproducible patterns are defined as disease endotypes. An endotype might consist of several intricated mechanisms that cannot be clearly separated into "pure single molecular mechanism" thus being a "complex endotype." The description of an endotype may rely on biomarkers, which can be the signature of a complex underlying pathway or a key molecule associated with or directly playing a role in a particular disease endotype. The Th2 type inflammation can be defined as a complex endotype in asthma and linked to mechanisms of disease development and response to treatment and to disease outcomes such as exacerbations and remodeling. The type 2 complex endotype in allergies and asthma includes innate lymphoid cells, T helper 2 cells, tissue eosinophilia, and IgE production. Currently, emerging endotype-driven strategies in asthma, particularly the development of biologicals that target a single molecular pathway, are being focused for solving individualized clinical problems on disease outcomes. Progress is also being made for endotyping rhinitis, chronic rhinosinusitis, and atopic dermatitis.
引用
收藏
页数:8
相关论文
共 77 条
[1]
Agache I, 2012, J INVEST ALLERG CLIN, V22, P419
[2]
Untangling asthma phenotypes and endotypes [J].
Agache, I. ;
Akdis, C. ;
Jutel, M. ;
Virchow, J. C. .
ALLERGY, 2012, 67 (07) :835-846
[3]
Persistent High FeNO Phenotype in Asthma [J].
Agache, I. O. ;
Ciobanu, C. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 127 (02) :AB4-AB4
[4]
Increased serum IL-17 is an independent risk factor for severe asthma [J].
Agache, Ioana ;
Ciobanu, Cristina ;
Agache, Costel ;
Anghel, Mariana .
RESPIRATORY MEDICINE, 2010, 104 (08) :1131-1137
[5]
From phenotypes to endotypes to asthma treatment [J].
Agache, Ioana O. .
CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 13 (03) :249-256
[6]
CD4+ invariant T-cell-receptor plus natural killer T cells in bronchial asthma. [J].
Akbari, O ;
Faul, JL ;
Hoyte, EG ;
Berry, GJ ;
Wahlström, J ;
Kronenberg, M ;
DeKruyff, RH ;
Umetsu, DT .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (11) :1117-1129
[7]
Endotypes and phenotypes of chronic rhinosinusitis: A PRACTALL document of the European Academy of Allergy and Clinical Immunology and the American Academy of Allergy, Asthma & Immunology [J].
Akdis, Cezmi A. ;
Bachert, Claus ;
Cingi, Cemal ;
Dykewicz, Mark S. ;
Hellings, Peter W. ;
Naclerio, Robert M. ;
Schleimer, Robert P. ;
Ledford, Dennis .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 131 (06) :1479-1490
[8]
Therapies for allergic inflammation: refining strategies to induce tolerance [J].
Akdis, Cezmi A. .
NATURE MEDICINE, 2012, 18 (05) :736-749
[9]
Akdis M, 2013, MIDDLETONS ALLERGY
[10]
Mechanisms of allergen-specific immunotherapy: Multiple suppressor factors at work in immune tolerance to allergens [J].
Akdis, Muebeccel ;
Akdis, Cezmi A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2014, 133 (03) :621-631