Leukocyte redistribution as immunological biomarker of corticosteroid resistance in severe asthma

• DOI: 10.1111/cea.14128
• Publication Date: 2022-03-19T13:30:12Z
• Authors: Carlos Cardoso‐Vi...; Tobias von Blumen...; Beate Rückert; Arturo O. Rinaldi; Ge Tan; Anita Dreher; Urszula Radzikowska; Günter Menz; Peter Schmid‐Gren...; Cezmi A. Akdis; Milena Sokolowska
• Keywords: 2403 Immunology; Environmental Biomarkers; Immunology; 10177 Dermatology Clinic; 610 Medicine & health; Original Articles; Allergens; Immunoglobulin E; Asthma; 3. Good health; Eosinophils; Leukocyte Count; 03 medical and health sciences; 0302 clinical medicine; 10183 Swiss Institute of Allergy and Asthma Research; Adrenal Cortex Hormones; 2723 Immunology and Allergy; Leukocytes; Immunology and Allergy; Humans; Biomarkers

AbstractBackgroundEarlier studies have suggested that the leukocyte redistribution can be considered as an immunological marker of the clinical response to corticosteroids (CS), representing an easy measurable potential biomarker in severe asthma.ObjectiveThe aim of this study was to determinate the utility of the leukocyte redistribution as a biomarker of disease heterogeneity in patients with severe asthma and as a bioindicator of potential CS resistance.MethodsWe developed an unbiased clustering approach based on the clinical data and the flow cytometry results of peripheral blood leukocyte phenotypes of 142 patients with severe asthma before and after systemic CS administration.ResultsBased on the differences in the blood count eosinophils, neutrophils and lymphocytes, together with the flow cytometry measurements of basic T cell, B cell and NK cell subpopulations before and after systemic CS administration, we identified two severe asthma clusters, which differed in the cell frequencies, response to CS and atopy status. Patients in cluster 1 had higher frequency of blood eosinophils at baseline, were sensitized to less allergens and had better steroid responsiveness, measured as the pronounced leukocyte redistribution after the administration of systemic CS. Patients in cluster 2 were determined by the higher frequency of B‐cells and stronger IgE sensitization status to the multiple allergens. They also displayed higher steroid resistance, as the clinical correlate for the lower leukocyte redistribution after administration of systemic CS.ConclusionThe flow cytometry‐based profiling of the basic populations of immune cells in the blood and its analysis before and after systemic corticosteroid administration could improve personalized treatment approaches in patients with severe asthma.