Rethinking neutrophils and eosinophils in chronic rhinosinusitis

被引:86
作者
Delemarre, Tim [1 ]
Bochner, Bruce S. [2 ]
Simon, Hans-Uwe [3 ,4 ,5 ]
Bachert, Claus [1 ,6 ,7 ]
机构
[1] Univ Ghent, Upper Airways Res Lab, Fac Med, Ghent, Belgium
[2] Northwestern Univ, Div Allergy & Immunol, Dept Med, Feinberg Sch Med, Chicago, IL USA
[3] Univ Bern, Inst Pharmacol, Bern, Switzerland
[4] Sechenov Univ, Dept Clin Immunol & Allergol, Moscow, Russia
[5] Kazan Fed Univ, Inst Fundamental Med & Biol, Lab Mol Immunol, Kazan, Russia
[6] Karolinska Inst, Div ENT Dis, CLINTEC, Stockholm, Sweden
[7] Sun Yat Sen Univ, Int Airway Res Ctr, Affiliated Hosp 1, Guangzhou, Peoples R China
基金
瑞士国家科学基金会;
关键词
Chronic rhinosinusitis; type; 2; inflammation; eosino-phils; neutrophils; activation; extracellular traps; Charcot-Leyden crystals; IL-17; biologicals; NASAL POLYPS; STAPHYLOCOCCUS-AUREUS; GENE-EXPRESSION; SINUS SURGERY; EXTRACELLULAR TRAPS; HEALING QUALITY; GM-CSF; INFLAMMATION; ASTHMA; DNA;
D O I
10.1016/j.jaci.2021.03.024
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Chronic rhinosinusitis (CRS) often is characterized by an eosinophilic inflammatory pattern, nowadays referred to as type 2 inflammation, although the mucosal inflammation is dominated by neutrophils in about a third of the patients. Neutrophils are typically predominant in 50% of patients with CRS without nasal polyps, but also are found to play a role in patients with severe type 2 CRS with nasal polyp disease. This review aims at summarizing the current understanding of the eosinophilic and neutrophilic inflammation in CRS pathophysiology, and provides a discussion of their reciprocal interactions and the clinical impact of the mixed presentation in patients with severe type 2 CRS with nasal polyps. A solid understanding of these interactions is of utmost importance when treating uncontrolled severe CRS with nasal polyps with biologicals that are preferentially directed toward type 2 inflammation. We here focus on recent findings on both eosinophilic and neutrophilic granulocytes, their subgroups and the activation status, and their interactions in CRS. (J Allergy Clin Immunol 2021;148:327-35.)
引用
收藏
页码:327 / 335
页数:9
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