Management Strategies to Reduce Exacerbations in non-T2 Asthma

被引:10
作者
Murphy, Ryan C. [1 ,2 ,3 ,4 ,5 ]
Pavord, Ian D. [2 ,3 ]
Alam, Rafeul [4 ]
Altman, Matthew C. [2 ,5 ]
机构
[1] Univ Washington, Divis Pulm Crit Care & Sleep Med, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Lung Biol, Dept Med, Seattle, WA 98195 USA
[3] Univ Oxford, NIHR Biomed Res Ctr, Dept Med, Respiratory Med Unit & Oxford Resp, Oxford, England
[4] Univ Colorado, Dept Med Natl Jewish Hlth, Div Allergy & Immunol, Denver, CO 80202 USA
[5] Univ Washington, Div Allergy & Immunol, Seattle, WA 98195 USA
关键词
Asthma; Airway inflammation; Non-T2; AIRWAY SMOOTH-MUSCLE; CROSS-SECTIONAL ANALYSIS; DOUBLE-BLIND; MAST-CELL; CIGARETTE-SMOKING; LUNG-FUNCTION; BRONCHIAL THERMOPLASTY; INFLAMMATORY SUBTYPES; UNCONTROLLED ASTHMA; TYPE-2; INFLAMMATION;
D O I
10.1016/j.jaip.2021.04.033
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
There have been considerable advances in our understanding of asthmatic airway inflammation, resulting in a paradigm shift of classifying individuals on the basis of either the presence or the absence of type 2 (T2) inflammatory markers. Several novel monoclonal antibody therapies targeting T2 cytokines have demonstrated significant clinical effects including reductions in acute exacerbations and improvements in asthma-related quality of life and lung function for individuals with T2-high asthma. However, there have been fewer advancements in developing therapies for those without evidence of T2 airway inflammation (so-called non-T2 asthma). Here, we review the heterogeneity of molecular mechanisms responsible for initiation and regulation of non-T2 inflammation and discuss both current and potential future therapeutic options for individuals with non-T2 asthma. (c) 2021 American Academy of Allergy, Asthma & Immunology (J Allergy Clin Immunol Pract 2021;9:2588-97)
引用
收藏
页码:2588 / 2597
页数:10
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