Revisiting Asian chronic rhinosinusitis in the era of type 2 biologics
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- Yin Yao
- Department of Otolaryngology‐Head and Neck Surgery Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China
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- Ming Zeng
- Department of Otolaryngology‐Head and Neck Surgery Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China
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- Zheng Liu
- Department of Otolaryngology‐Head and Neck Surgery Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China
説明
<jats:title>Abstract</jats:title><jats:p>Chronic rhinosinusitis (CRS) is a highly heterogeneous disorder exhibiting considerable epidemiological, clinical and immunopathological variations across patients with distinct ethnic backgrounds and in different geographic locations. Asian CRS patients present less eosinophilic and type 2 (T2) inflammation, but more prominent neutrophilic inflammation compared with patients in Western countries. Although several biologics targeting important elements of T2 inflammation, such as IL‐4, IL‐5, IL‐13 and IgE, demonstrate promising benefit for Caucasian patients with recurrent nasal polyps, their efficacy in Asian patients remains poorly defined. The distinct endotypes in Asian patients warrant the identification and selection of patients who would benefit from T2 biologics in Asian countries. Additionally, developing novel treatments targeting neutrophilic, type 1, and type 3 inflammation may benefit approximately 50% of Asian CRS patients with non‐T2 inflammation. In this review, we summarized and discussed recent progress in the study of Asian CRS endotypes in comparison with those in patients in Western countries, and the methods of identifying Asian patients with eosinophilic or T2 inflammation. T2 biologic treatment of Asian CRS patients, potential therapeutic candidates targeting non‐T2 inflammation in Asian CRS patients and the progress on developing other T2 biologics were discussed.</jats:p>
収録刊行物
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- Clinical & Experimental Allergy
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Clinical & Experimental Allergy 52 (2), 231-243, 2021-12-09
Wiley