# Marked Clinical and Functional Response to Tezepelumab After Failure of Anti-Interleukin-5 (Anti-IL-5) Therapy in Severe Asthma

**Authors:** Makoto Fujimoto, Toyoshi Yanagihara, Yuka Sakaki, Masaki Fujita

PMC · DOI: 10.7759/cureus.103648 · Cureus · 2026-02-15

## TL;DR

An elderly woman with severe asthma showed significant improvement after switching from mepolizumab to tezepelumab, even after years of persistent symptoms.

## Contribution

Demonstrates that tezepelumab can induce functional recovery in severe asthma after anti-IL-5 therapy failure.

## Key findings

- The patient's FEV₁ improved dramatically from 45.7% to 103% predicted within two months of tezepelumab treatment.
- Her symptoms and airflow limitation resolved, with a near-normalization of the flow-volume loop.
- This case challenges the notion that chronic airflow limitation in severe asthma is always irreversible.

## Abstract

Biologics targeting type 2 inflammation, including anti-interleukin-5 (anti-IL-5) antibodies, have improved outcomes in severe asthma, but some patients remain symptomatic with apparently persistent severe airflow limitation. We report an 86-year-old woman with long-standing severe asthma who initially had high blood eosinophil counts and serum immunoglobulin E (IgE) levels. She responded to mepolizumab for years, while airflow limitation persisted. She developed an exacerbation seven years after mepolizumab initiation despite ongoing mepolizumab and inhaled triple therapy, while type 2 biomarkers normalized. She continued to experience dyspnea with triggers such as cold air and pollen. After switching from mepolizumab to tezepelumab, her symptoms rapidly resolved; forced expiratory volume in one second (FEV₁) increased from 0.64 L (45.7% predicted) to 1.45 L (103% predicted) within two months, and the concave flow-volume loop became almost normal. This case suggests that chronic airflow limitation in severe asthma is not always irreversible and that switching to tezepelumab may induce dramatic functional recovery even after anti-IL-5 therapy.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}
- **Diseases:** type 2 inflammation (MESH:D007249), Asthma (MESH:D001249), airflow limitation (MESH:D029424), dyspnea (MESH:D004417)
- **Chemicals:** mepolizumab (MESH:C434107), Tezepelumab (MESH:C000622721)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12994096/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12994096/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12994096/full.md

---
Source: https://tomesphere.com/paper/PMC12994096