# Biologics for eosinophilic COPD: current applications and future prospects

**Authors:** Qi Qi, Wenbei Peng, Bohan Yang, Shijie Liu, Ying Pu, Qiong Zhou

PMC · DOI: 10.3389/fimmu.2026.1722371 · Frontiers in Immunology · 2026-02-26

## TL;DR

This review discusses new biologics for COPD patients with eosinophilic inflammation and highlights the importance of biomarkers for better treatment.

## Contribution

The paper reviews emerging biologics targeting type 2 inflammation in COPD and emphasizes the role of biomarkers.

## Key findings

- Eosinophilic COPD patients remain at risk of exacerbations despite standard therapy.
- Monoclonal antibodies targeting type 2 pathways show promise in treating eosinophilic COPD.
- Accurate biomarkers are essential for identifying patients who may benefit from these biologics.

## Abstract

Chronic obstructive pulmonary disease (COPD) is a heterogeneous pulmonary disorder characterized by persistent airflow limitation and symptoms of progressive dyspnea, cough, and sputum. While traditionally linked to type 1 immunity, a significant subset of patients presents with eosinophil-predominant type 2 inflammation. These individuals remain at risk of exacerbations despite receiving triple therapy, underscoring the need for novel biologics targeting type 2 pathways. Monoclonal antibodies against targets such as IL-5/IL-5Rα, IL-4, IL-13, IL-33/ST-2, and thymic stromal lymphopoietin (TSLP) have shown considerable promise. Therefore, the identification of accurate and accessible biomarkers for type 2 inflammation is crucial. This review summarizes the current applications and future prospects of emerging biologics in eosinophilic COPD, with a specific focus on the role of biomarkers.

## Linked entities

- **Proteins:** IL5 (interleukin 5), IL5RA (interleukin 5 receptor subunit alpha), IL4 (interleukin 4), IL13 (interleukin 13), IL33 (interleukin 33), ST2 (suppression of tumorigenicity 2), TSLP (thymic stromal lymphopoietin)
- **Diseases:** COPD (MONDO:0005002), chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Genes:** TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5RA (interleukin 5 receptor subunit alpha) [NCBI Gene 3568] {aka CD125, CDw125, HSIL5R3, IL5R}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, ST2 (suppression of tumorigenicity 2) [NCBI Gene 6761]
- **Diseases:** cough (MESH:D003371), type 2 inflammation (MESH:D007249), dyspnea (MESH:D004417), pulmonary disorder (MESH:D008171), COPD (MESH:D029424)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12979430/full.md

## References

107 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979430/full.md

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Source: https://tomesphere.com/paper/PMC12979430