Chronic Rhinosinusitis with Nasal Polyps and Asthma

被引:266
作者
Laidlaw, Tanya M. [1 ,2 ]
Mullol, Joaquim [3 ]
Woessner, Katharine M. [4 ]
Amin, Nikhil [5 ]
Mannent, Leda P. [6 ]
机构
[1] Brigham & Womens Hosp, Div Allergy & Clin Immunol, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Univ Barcelona, Hosp Clin, CIBERES, IDIBAPS, Barcelona, Spain
[4] Scripps Med Clin Grp, Div Allergy Asthma & Immunol, San Diego, CA USA
[5] Regeneron Pharmaceut Inc, Tarrytown, NY USA
[6] Sanofi R&D, Chilly Mazarin, France
关键词
Asthma; Aspirin/NSAID-exacerbated respiratory disease; Chronic rhinosinusitis with nasal polyps; Type; 2; inflammation; EXACERBATED RESPIRATORY-DISEASE; QUALITY-OF-LIFE; ENDOSCOPIC SINUS SURGERY; INNATE LYMPHOID-CELLS; ALLERGIC RHINITIS; AIRWAY INFLAMMATION; PROSTAGLANDIN E-2; MAST-CELL; ASPIRIN; IMPACT;
D O I
10.1016/j.jaip.2020.09.063
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Patients with chronic rhinosinusitis with nasal polyps (CRSwNP) characterized by a type 2 immune signature often have severe and recurrent disease. Lower airway conditions such as asthma are common comorbidities and share similar pathophysiology. CRSwNP with asthma is characterized by tissue eosinophilia and high local IgE levels. Clinically, CRSwNP with comorbid asthma is associated with more severe sinonasal symptoms and worse quality of life, and it is more difficult to treat both medically and surgically. Asthma in the presence of nasal polyposis is also more difficult to control, being more exacerbation prone, with increased airway obstruction and more extensive eosinophilic inflammation. Aspirin/nonsteroidal anti-inflammatory drug-exacerbated respiratory disease (AERD) is a recognized phenotype of CRSwNP with comorbid asthma. Patients with CRSwNP with comorbid AERD are among those with the most severe and difficult-to-treat disease, and tend to have severe NP. The shared pathophysiology of the upper and lower airways has important implications for both the diagnosis and management of respiratory comorbidities. However, in clinical practice, the nose and lungs are often treated as separate entities. The underlying systemic inflammatory link between CRSwNP and asthma provides a compelling rationale for systemic treatment with novel biologics targeting shared underlying type 2 inflammatory pathways. (C) 2020 American Academy of Allergy, Asthma & Immunology
引用
收藏
页码:1133 / 1141
页数:9
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