Case Report: Tezepelumab as rescue therapy in near-fatal asthma requiring extracorporeal membrane oxygenation

BACKGROUND: Tezepelumab, an anti-thymic stromal lymphopoietin (TSLP) monoclonal antibody, reduces exacerbations across asthma phenotypes, but its role in status asthmaticus and near-fatal exacerbations requiring veno-venous extracorporeal membrane oxygenation (VV-ECMO) is unclear. METHODS AND RESULTS: We report three patients (17, 22, 57 years) with therapy-refractory hypercapnic respiratory failure initiated on VV-ECMO who received tezepelumab 210 mg within 24 h. Tidal volume and minute ventilation increased within 24-72 h, permitting decannulation by days 12-15 and ventilator weaning by days 17-28. Two patients had elevated IgE; one had normal blood eosinophils/IgE. No immediate drug-related adverse events occurred. Follow-up demonstrated lung-function recovery; one patient required escalation of maintenance therapy for persistent symptoms. CONCLUSION: In this small series, adjunctive tezepelumab during VV-ECMO-supported status asthmaticus appeared safe and potentially beneficial adjunctive therapy during near-fatal asthma requiring VV-ECMO. Randomized controlled studies are needed to determine the impact of TSLP inhibition on recovery time, ventilation duration, and mortality in this setting.

  • Oruqaj, G.
  • Bewersdorff, J.
  • Litzlbauer, D.
  • Wolff, M.
  • Sander, M.
  • Seeger, W.
  • Grimminger, F.
  • Hecker, M.
  • Tello, K.
  • Vadasz, I.

Keywords

  • Humans
  • *Antibodies, Monoclonal, Humanized/therapeutic use
  • *Extracorporeal Membrane Oxygenation
  • Middle Aged
  • Male
  • Female
  • *Asthma/therapy
  • Young Adult
  • Treatment Outcome
  • Adolescent
  • *Anti-Asthmatic Agents/therapeutic use
  • *Status Asthmaticus/therapy
  • Adult
  • Cytokines/antagonists & inhibitors
  • Thymic Stromal Lymphopoietin
  • Ecmo
  • Icu
  • Tslp
  • Tezepelumab
  • status asthmaticus
Publication details
DOI: 10.3389/fimmu.2026.1722963
Journal: Front Immunol
Pages: 1722963
Work Type: Original
Access number: 41766851
See publication on PubMed
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