Biologic and New Therapies in Asthma

被引:32
|
作者
Tabatabaian, Farnaz [1 ]
Ledford, Dennis K. [1 ,2 ]
Casale, Thomas B. [1 ,3 ]
机构
[1] Univ S Florida, Dept Internal Med, Morsani Coll Med, Div Allergy & Immunol, 13330 USF Laurel Dr 5th Floor,MDC 80, Tampa, FL 33612 USA
[2] Univ S Florida, James A Haley VA Hosp, Morsani Coll Med, Div Allergy & Immunol,Dept Internal Med, 13000 Bruce B,Downs Blvd, Tampa, FL 33612 USA
[3] Univ S Florida, Morsani Coll Med, Dept Internal Med, Div Allergy & Immunol, 12901 Bruce B Downs Blvd,MDC 19, Tampa, FL 33612 USA
关键词
Biologics; Asthma; Anti-IL-5; Anti-IL-13; Anti-IL-4; Th2; CRTH2; Anti-IgE; EXHALED NITRIC-OXIDE; SEVERE EOSINOPHILIC ASTHMA; ALPHA MONOCLONAL-ANTIBODY; DOUBLE-BLIND; INHALED CORTICOSTEROIDS; PERSISTENT ASTHMA; RANDOMIZED-TRIAL; PLACEBO; MEPOLIZUMAB; SAFETY;
D O I
10.1016/j.iac.2017.01.007
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Several biologics are currently FDA approved for asthma that target Th2 high patients. Unfortunately, 50% of patients with severe asthma do not fit this phenotype of disease and have fewer effective therapeutic options. In the clinical setting, total IgE, FeNO and peripheral blood eosinophils are important tools in defining Th2 high patients with asthma. However, precise biomarkers to predict better response to one specific Th2 high asthma therapy versus another is lacking. It is important to recognize that none of the current medications targeting the Th2 pathway induces persistent immunomodulation or remission.
引用
收藏
页码:329 / +
页数:17
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