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Mepolizumab is a monoclonal antibody used to treat severe eosinophilic asthma and other eosinophilic conditions. It works by blocking interleukin-5, thereby reducing eosinophil levels in the blood.
Mepolizumab is a monoclonal antibody used to treat severe eosinophilic asthma and other eosinophilic conditions. It works by blocking interleukin-5, thereby reducing eosinophil levels in the blood.
Mepolizumab is a humanized monoclonal antibody that targets interleukin-5 (IL-5), a signaling protein (cytokine) that plays a key role in the production, maturation, and survival of eosinophils – a type of white blood cell that, when overactivated, can trigger damaging inflammatory responses. Mepolizumab is marketed under the brand name Nucala® and is approved by regulatory authorities including the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA).
Mepolizumab binds specifically to interleukin-5, preventing it from attaching to its receptor on the surface of eosinophils. This leads to a significant reduction in circulating and tissue eosinophil counts. By inhibiting the IL-5 pathway, the drug directly reduces eosinophilic inflammation, which is a key driver in several chronic conditions.
Mepolizumab is approved for the following conditions:
Mepolizumab is administered as a subcutaneous injection (under the skin), typically once every four weeks. The standard dose for severe eosinophilic asthma is 100 mg in adults and adolescents, and 40 mg in children aged 6 to 11 years. For EGPA and HES, a higher dose of 300 mg (given as three separate 100 mg injections) is used. After proper training, patients may self-administer the injection at home.
Mepolizumab is generally well tolerated. The most common side effects include:
Rare but serious side effects include anaphylaxis (severe allergic reaction), which requires immediate medical attention. Because eosinophils also play a role in defending against parasitic infections, mepolizumab may increase susceptibility to such infections in patients living in or traveling to endemic areas.
Mepolizumab represents a significant advance in biologic therapy for respiratory and eosinophilic diseases. It is indicated when conventional treatments such as inhaled corticosteroids, long-acting beta-2 agonists, or oral corticosteroids are insufficient. Clinical trials have demonstrated that mepolizumab significantly reduces the rate of asthma exacerbations, improves lung function, and enhances patients quality of life. Additionally, it has been shown to have an oral corticosteroid-sparing effect, helping to reduce long-term steroid-related side effects.
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