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Omalizumab Restores Response to Corticosteroids in Patients with Eosinophilic Chronic Rhinosinusitis and Severe Asthma

Authors :
Akira Kanda
Hiroshi Iwai
Linh Manh Nguyen
Hanh Hong Chu
Akitoshi Mitani
Yoshiki Kobayashi
Mikiya Asako
Kensuke Suzuki
Dan Van Bui
Yasutaka Yun
Source :
Biomedicines, Vol 9, Iss 787, p 787 (2021), Biomedicines, Volume 9, Issue 7
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Eosinophilic chronic rhinosinusitis (ECRS), which is a subgroup of chronic rhinosinusitis with nasal polyps, is characterized by eosinophilic airway inflammation extending across both the upper and lower airways. Some severe cases are refractory even after endoscopic sinus surgery, likely because of local steroid insensitivity. Although real-life studies indicate that treatment with omalizumab for severe allergic asthma improves the outcome of coexistent ECRS, the underlying mechanisms of omalizumab in eosinophilic airway inflammation have not been fully elucidated. Twenty-five patients with ECRS and severe asthma who were refractory to conventional treatments and who received omalizumab were evaluated. Nineteen of twenty-five patients were responsive to omalizumab according to physician-assessed global evaluation of treatment effectiveness. In the responders, the levels of peripheral blood eosinophils and fractionated exhaled nitric oxide (a marker of eosinophilic inflammation) and of CCL4 and soluble CD69 (markers of eosinophil activation) were reduced concomitantly with the restoration of corticosteroid sensitivity. Omalizumab restored the eosinophil-peroxidase-mediated PP2A inactivation and steroid insensitivity in BEAS-2B. In addition, the local inflammation simulant model using BEAS-2B cells incubated with diluted serum from each patient confirmed omalizumab’s effects on restoration of corticosteroid sensitivity via PP2A activation<br />thus, omalizumab could be a promising therapeutic option for refractory eosinophilic airway inflammation with corticosteroid resistance.

Details

Language :
English
ISSN :
22279059
Volume :
9
Issue :
787
Database :
OpenAIRE
Journal :
Biomedicines
Accession number :
edsair.doi.dedup.....5e77f60c4ae9774e41297cd822a211ae