Abstract | INTRODUCTION: Five percent of asthmatics have severe symptoms despite high doses of inhaled (ICS) or additional oral corticosteroids (OCS): these patients have high morbidity, risk for asthma death, and account for half of asthma healthcare spending. A subgroup (20 - 40%) of these has persistent airway eosinophilia and frequent exacerbations. Mepolizumab is a humanized monoclonal antibody that blocks binding of the key cytokine implicated specifically in eosinophil maturation and survival, interleukin-5, to its receptor. AREAS COVERED: Pharmacology, Phase I/IIa and Phase II/III studies of mepolizumab for asthma. Mepolizumab depleted blood and sputum eosinophils and partially reduced airway and bone marrow eosinophils. It also reduced airway remodeling. In unselected patients with moderate/severe asthma there was no clinically significant effect on lung function, but a trend to reduced exacerbation rates. When patients were selected for persistent sputum eosinophilia despite high-dose ICS/OCS, and frequent exacerbations, mepolizumab reduced exacerbations by 50%. EXPERT OPINION:
Mepolizumab can reduce exacerbation rates in the severe asthma cohort who have eosinophilic airway inflammation despite corticosteroid treatment. This may be 30% of severe asthmatics and represents a new and important treatment option. Further studies need to confirm efficacy and indications for asthma (and other eosinophilic airway disease), and to examine clinical consequences of reducing remodeling.
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Authors | Douglas S Robinson |
Journal | Expert opinion on biological therapy
(Expert Opin Biol Ther)
Vol. 13
Issue 2
Pg. 295-302
(Feb 2013)
ISSN: 1744-7682 [Electronic] England |
PMID | 22998420
(Publication Type: Journal Article)
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Chemical References |
- Antibodies, Monoclonal, Humanized
- Interleukin-5
- mepolizumab
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Topics |
- Antibodies, Monoclonal, Humanized
(immunology, pharmacokinetics, therapeutic use)
- Asthma
(drug therapy, immunology)
- Humans
- Interleukin-5
(immunology)
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