Abstract

Background: Asthma is a heterogeneous syndrome with a broad clinical spectrum and high drug response variability. The inflammatory response in asthma involves multiple effector cells and mediator molecules. Based on asthma immunopathogenesis, precision medicine can be a promising strategy for identifying biomarkers. Biologic therapies acting on the IL-5/IL-5 receptor axis have been developed. IL-5 promotes proliferation, differentiation and activation of eosinophils by binding to the IL-5 receptor, located on the surface of eosinophils and basophils. This study aimed to investigate the expression of IL5RA in patients with several types of asthma and its expression after treatment with benralizumab, a biologic directed against IL-5 receptor subunit alpha.Methods: Sixty peripheral blood samples, 30 from healthy controls and 30 from asthmatic patients, were selected for a transcriptomic RNAseq study. Differential expression analysis was performed by statistical assessment of fold changes and P-values. A validation study of IL5RA expression was developed using qPCR in 100 controls and 187 asthmatic patients. The effect of benralizumab on IL5RA expression was evaluated in five patients by comparing expression levels between pretreatment and after 3 months of treatment. The IL5RA mRNA levels were normalized to GAPDH and TBP expression values for each sample. Calculations were made by the comparative ΔΔCt method. All procedures followed the MIQE guidelines.Results:IL5RA was one of the most differentially overexpressed coding transcripts in the peripheral blood of asthmatic patients (P = 8.63E-08 and fold change of 2.22). In the qPCR validation study, IL5RA expression levels were significantly higher in asthmatic patients than in controls (P < 0.001). Significant expression differences were present in different asthmatic types. In the biological drug study, patients treated with benralizumab showed a significant decrease in IL5RA expression and blood eosinophil counts. A notable improvement in ACT and lung function was also observed in these patients.Conclusions: These results indicate that IL5RA is overexpressed in patients with different types of asthma. It could help identify which asthmatic patients will respond more efficiently to benralizumab, moving toward a more personalized asthma management. Although further studies are required, IL5RA could play a role as a biomarker and pharmacogenetic factor in asthma.

Highlights

  • Asthma is a chronic inflammatory disease of the airways affecting more than 300 million people worldwide, and its prevalence is increasing, becoming a health and economic problem [1]

  • The characteristic inflammatory pattern in most asthmatic patients includes an increase in type 2 helper T (Th2) lymphocytes, eosinophils, basophils, mast cells and type 2 innate lymphoid cells (ILC2)

  • The present study aims to investigate the expression of IL5RA in patients with different types of asthma and its role as a possible biomarker of response to treatment with benralizumab

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Summary

Introduction

Asthma is a chronic inflammatory disease of the airways affecting more than 300 million people worldwide, and its prevalence is increasing, becoming a health and economic problem [1] It is defined by variable expiratory airflow limitation and respiratory symptoms such as wheeze, cough and shortness of breath, which vary in frequency and intensity [2]. Asthma is recognized as a heterogeneous syndrome with different underlying disease processes, determined by complex interactions between genetic and environmental factors This variety of interactions results in different clinical presentations, phenotypes and response to treatment [3]. The characteristic inflammatory pattern in most asthmatic patients includes an increase in type 2 helper T (Th2) lymphocytes, eosinophils, basophils, mast cells and type 2 innate lymphoid cells (ILC2) These effector cells release numerous mediating molecules that cause disease symptoms [5]. This study aimed to investigate the expression of IL5RA in patients with several types of asthma and its expression after treatment with benralizumab, a biologic directed against IL-5 receptor subunit alpha

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