Benralizumab for Prednisone-Dependent Eosinophilic Asthma Associated With Novel STAT3 Loss of Function Mutation

Chest. 2021 Apr;159(4):e181-e184. doi: 10.1016/j.chest.2020.11.042. Epub 2021 Apr 6.

Abstract

Some severe asthmatic patients experience frequent bacterial respiratory tract infections, which contribute significantly to their disease burden, and often are attributed to their use of systemic corticosteroids and comorbid bronchiectasis. We report a case of a 58-year-old woman who had prednisone-dependent asthma and exacerbations with intense mixed eosinophilic and neutrophilic bronchitis. Autosomal dominant hyper-IgE syndrome, which is a primary immunodeficiency characterized by elevated IgE, eosinophilia, and recurrent infections, caused by a novel pathogenic mutation in STAT3 was identified as the cause of her airway disease. We believe that this is the first report of the demonstration of an IL-5 driven eosinophilia that is associated with a STAT3 mutation that was treated successfully with an anti-IL5 biological.

Keywords: STAT3; asthma; benralizumab; eosinophilia; hyper-IgE syndrome.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Asthmatic Agents / therapeutic use
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Asthma / drug therapy*
  • Asthma / genetics
  • Asthma / metabolism
  • DNA / genetics*
  • DNA Mutational Analysis
  • Disease Progression
  • Drug Therapy, Combination
  • Female
  • Glucocorticoids / therapeutic use
  • Humans
  • Loss of Function Mutation*
  • Middle Aged
  • Prednisone / therapeutic use*
  • Pulmonary Eosinophilia / drug therapy*
  • Pulmonary Eosinophilia / genetics
  • Pulmonary Eosinophilia / metabolism
  • STAT3 Transcription Factor / genetics*
  • STAT3 Transcription Factor / metabolism

Substances

  • Anti-Asthmatic Agents
  • Antibodies, Monoclonal, Humanized
  • Glucocorticoids
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • benralizumab
  • DNA
  • Prednisone