Changes in Type 2 Biomarkers After Anti-IL5 Treatment in Patients With Severe Eosinophilic Asthma

Patients with severe eosinophilic asthma (SEA) suffer from frequent asthma exacerbations, where eosinophils are major effector cells in airway inflammation, and anti-interleukin (IL)-5 becomes an effective treatment modality to control eosinophilic inflammation of SEA. Fifteen patients with SEA who...

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Veröffentlicht in:Allergy, asthma & immunology research asthma & immunology research, 2021-03, Vol.13 (2), p.330-338
Hauptverfasser: Jang, Jae Hyuk, Woo, Seong Dae, Lee, Youngsoo, Kim, Chang Keun, Shin, Yoo Seob, Ye, Young Min, Park, Hae Sim
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Sprache:eng
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Zusammenfassung:Patients with severe eosinophilic asthma (SEA) suffer from frequent asthma exacerbations, where eosinophils are major effector cells in airway inflammation, and anti-interleukin (IL)-5 becomes an effective treatment modality to control eosinophilic inflammation of SEA. Fifteen patients with SEA who had been treated with anti-IL5 (reslizumab, 100 mg monthly intravenously) for 6 months at Ajou University Hospital (Suwon, Korea) were enrolled in this study. Clinical parameters, including total blood eosinophil count (TEC), FEV1%, fractional exhaled nitric oxide (FeNO) levels, and serum biomarkers such as eosinophil-derived neurotoxin (EDN), periostin (PON), and transforming growth factor-β1 (TGF-β1), were analyzed. EDN levels and TEC decreased significantly after 1 month of treatment ( < 0.05 for both), while no changes were noted in FeNO/PON/TGF-β1 levels. FEV1% increased after 2 months of treatment ( < 0.05). A positive correlation was observed between TEC and EDN levels ( = 0.60, = 0.02). Significant negative correlations were noted between age and TEC/EDN levels ( = -0.57, = 0.02 and = -0.56, = 0.03, respectively). Baseline TEC was higher in the EDN-responder group (≥75% decrease) than in the non-responder group ( = 0.06) with a positive correlation between %reduction in EDN and TEC ( = 0.67, = 0.01). The onset age was younger and asthma duration was longer in the FEV1%-non-responder group (
ISSN:2092-7355
2092-7363
DOI:10.4168/aair.2021.13.2.330