Immunoregulation of asthma by type 2 cytokine therapies: Treatments for all ages?

被引:3
|
作者
Saglani, Sejal [1 ,2 ]
Yates, Laura [1 ]
Lloyd, Clare M. [1 ]
机构
[1] Imperial Coll London, Natl Heart & Lung Inst, London, England
[2] Guys & St Thomas NHS Fdn Trust, Royal Brompton & Harefield Hosp, London, England
关键词
Asthma; Asthma biologics; Immunoregulation; type; 2; DOUBLE-BLIND; EOSINOPHIL MIGRATION; UNCONTROLLED ASTHMA; IL-4; RECEPTOR; EFFICACY; INFLAMMATION; BENRALIZUMAB; MEPOLIZUMAB; ADULTS; INTERLEUKIN-4;
D O I
10.1002/eji.202249919
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Asthma is classically considered to be a disease of type 2 immune dysfunction, since many patients exhibit the consequences of excess secretion of cytokines such as IL-4, IL-5, and IL-13 concomitant with inflammation typified by eosinophils. Mouse and human disease models have determined that many of the canonical pathophysiologic features of asthma may be caused by these disordered type 2 immune pathways. As such considerable efforts have been made to develop specific drugs targeting key cytokines. There are currently available multiple biologic agents that successfully reduce the functions of IL-4, IL-5, and IL-13 in patients, and many improve the course of severe asthma. However, none are curative and do not always minimize the key features of disease, such as airway hyperresponsiveness. Here, we review the current therapeutic landscape targeting type 2 immune cytokines and discuss evidence of efficacy and limitations of their use in adults and children with asthma.
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页数:11
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