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        <datestamp>2026-10-01T17:11:10Z</datestamp>
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          <dc:title>Exacerbation and glucocorticoid toxicity profile in patients receiving mepolizumab for severe eosinophilic asthma</dc:title>
          <dc:creator>Pamela Jane McDowell (13406403)</dc:creator>
          <dc:subject>PUREID: 297759532</dc:subject>
          <dc:subject>Asthma</dc:subject>
          <dc:subject>eosinophilic</dc:subject>
          <dc:subject>T2 high</dc:subject>
          <dc:subject>monoclonal antibodies</dc:subject>
          <dc:description>The treatment of patients with severe eosinophilic asthma has been transformed with the arrival of biological drugs targeting the type 2 cytokine pathway. One of these drugs is mepolizumab, a humanised monoclonal antibody against the eosinophil activating cytokine, interleukin (IL)-5, has consistently been shown to lead to a 50% reduction in exacerbation rate, when compared with placebo, and facilitates the weaning of maintenance oral corticosteroids (OCS) in patients with severe eosinophilic asthma. &lt;br&gt;&lt;br&gt;This works seeks to address two questions that arise from treatment with this novel monoclonal antibody:&lt;br&gt;&lt;br&gt;1. What is the inflammatory phenotype and the physiological characteristics of the residual asthma exacerbations that occur in patients with severe eosinophilic asthma treated with anti-IL5 monoclonal antibodies?&lt;br&gt;&lt;br&gt;2. To quantify toxicity associated with OCS treatment in severe eosinophilic asthmatics, and assess change in OCS-related toxicity after 1 year's treatment with mepolizumab and subsequent reduction in OCS, both through weaning of maintenance OCS and reduction in OCS for asthma exacerbations.</dc:description>
          <dc:date>2026-10-01T17:11:10Z</dc:date>
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          <dc:identifier>10.17034/32632482.v1</dc:identifier>
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