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Abstract
This review will describe the structure and function of the eosinophil. The roles
of several relevant cell surface molecules and receptors will be discussed. We will
also explore the systemic and local processes triggering eosinophil differentiation,
maturation, and migration to the lungs in asthma, as well as the cytokine-mediated
pathways that result in eosinophil activation and degranulation, i.e., the release
of multiple pro-inflammatory substances from eosinophil-specific granules, including
cationic proteins, cytokines, chemokines growth factors, and enzymes. We will discuss
the current understanding of the roles that eosinophils play in key asthma processes
such as airway hyperresponsiveness, mucus hypersecretion, and airway remodeling, in
addition to the evidence relating to eosinophil–pathogen interactions within the lungs.
Benralizumab is a humanised, afucosylated, anti-interleukin-5 receptor α monoclonal antibody that induces direct, rapid, and nearly complete depletion of eosinophils. We aimed to assess the efficacy and safety of benralizumab as add-on therapy for patients with severe, uncontrolled asthma and elevated blood eosinophil counts.
Eosinophilia is associated with worsening asthma severity and decreased lung function, with increased exacerbation frequency. We assessed the safety and efficacy of benralizumab, a monoclonal antibody against interleukin-5 receptor α that depletes eosinophils by antibody-dependent cell-mediated cytotoxicity, for patients with severe, uncontrolled asthma with eosinophilia.
[1]1Imperial College London , London, United Kingdom
[2]2Royal Brompton and Harefield NHS Foundation Trust , London, United Kingdom
Author notes
Edited by: Mats W. Johansson, University of Wisconsin-Madison, United States
Reviewed by: Praveen Akuthota, University of California San Diego, United States;
Christophe Von Garnier, University Children’s Hospital Bern, Switzerland; Eleni Papakonstantinou,
Aristotle University of Thessaloniki, Greece
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