TB Research

A single-center observational study assessing response to mepolizumab in severe eosinophilic asthma

Nadia Suray Tan, Manali Mukherjee, Sheau Yng Lim, Chung Hwee Thiam, W.S. Daniel Tan, W.S. Fred Wong, Parameswaran Nair, Véronique Angeli, et al. (9 authors)

Abstract

<b>Background:</b> Mepolizumab reduces blood and sputum eosinophils and can reduce exacerbations in severe eosinophilic asthma (SEA). However only 50% of prednisolone-dependent SEA patients are able to reduce their maintenance prednisolone. <b>Method:</b> We measured sputum and blood eosinophil counts and asthma control test (ACT) in 6 SEA patients on monthly Mepolizumab injection at baseline, 3, 6 and 12month of treatment. Suboptimal treatment responsiveness is defined as sputum eosinophil counts &gt; 3% after 4 months of treatment and at least one of the following: (1) ACT score &lt; 20 2) reduction in prednisolone dosage by &lt;50% 3) ≥1 exacerbation requiring prednisolone burst. <b>Results:</b> Four out of the 6 SEA patients are prednisolone-dependent (medium dose 5mg daily); the remaining 2 are on fluticasone &gt; 500mcg daily. Good treatment response was present in 3 patients and only 1 was prednisolone-dependent (table 1). Though they were able to reduce exacerbations by 66-83%, their maintenance prednisolone dose was reduced by only 0-33%. Sputum lymphocyte differential count increased in all 6 patients despite the decrease in blood and sputum eosinophil counts (Table 1). In patients with suboptimal response, their sputum showed an increase in total IgG, IgG2, anti-eosinophil peroxidase and anti-nuclear antibody, suggesting the development of an autoimmune response in severe prednisolone-dependent patients hindering treatment response.

MeSH terms

  • Medicine
  • Sputum
  • Prednisolone
  • Mepolizumab
  • Eosinophil
  • Exacerbation
  • Asthma
  • Internal medicine
  • Fluticasone
  • Immunology
  • Eosinophil cationic protein
  • Gastroenterology