# Interleukin-37 in respiratory diseases: molecular mechanisms and immune modulation

**Authors:** Jing Cao, Kun He, Zixiao Chen, Haibo Xu, Jiaona Wei, Xixin Yan, Beibei Song

PMC · DOI: 10.3389/fimmu.2025.1675791 · Frontiers in Immunology · 2025-11-10

## TL;DR

This paper reviews how IL-37, an anti-inflammatory protein, helps protect against various respiratory diseases by modulating immune responses and inflammation.

## Contribution

The paper systematically summarizes the molecular mechanisms of IL-37 and its therapeutic potential in respiratory diseases.

## Key findings

- IL-37 reduces asthma severity by inhibiting Th2/Th17 responses and epithelial alarmins.
- In viral infections like COVID-19 and influenza, IL-37 mitigates hyperinflammation and viral replication.
- IL-37 suppresses lung cancer progression and fibrosis by reducing tumor growth and collagen deposition.

## Abstract

Interleukin-37 (IL-37) is a potent anti-inflammatory cytokine that plays a crucial protective role in cancer, autoimmune diseases, and inflammatory diseases though its unique dual intracellular and extracellular action pathways. This review highlights the significance of IL-37 in common respiratory diseases. Specifically, IL-37 can alleviate asthma by inhibiting Th2/Th17 immune responses, inhibiting the release of epithelial-derived alarmins (TSLP and IL-33), and attenuating airway remodeling. In pulmonary infections, IL-37 modulates host responses by mitigating virus-induced hyperinflammation and inhibiting viral replication, as observed in COVID-19 and influenza, while also regulating immunopathology in Mycobacterium tuberculosis and fungal infections. Moreover, in non-small cell lung cancer (NSCLC), IL-37 directly suppresses tumor proliferation and migration, and restrains tumor progression through immunomodulation and angiogenesis regulation. In pulmonary fibrosis, IL-37 reduces collagen deposition and promotes autophagy, thereby counteracting interstitial fibrosis. Collectively, these findings demonstrate that IL-37 serves as a crucial immunomodulator in respiratory diseases, and targeting IL-37 offers novel insights and strategic opportunities for clinical intervention. This review systematically summarizes the molecular mechanisms of IL-37 and discusses its clinical therapeutic potential.

## Linked entities

- **Genes:** IL37 (interleukin 37) [NCBI Gene 27178]
- **Proteins:** TSLP (thymic stromal lymphopoietin), IL33 (interleukin 33)
- **Diseases:** asthma (MONDO:0004979), non-small cell lung cancer (MONDO:0005233), pulmonary fibrosis (MONDO:0002771), influenza (MONDO:0005812), COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** respiratory diseases (MESH:D012140), NSCLC (MESH:D002289), autoimmune diseases (MESH:D001327), inflammatory (MESH:D007249), influenza (MESH:D007251), COVID-19 (MESH:D000086382), pulmonary infections (MESH:D012141), pulmonary fibrosis (MESH:D011658), cancer (MESH:D009369), asthma (MESH:D001249), fungal infections (MESH:D009181), interstitial fibrosis (MESH:D005355), Mycobacterium tuberculosis (MESH:D014376)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12640846/full.md

## References

142 references — full list in the complete paper: https://tomesphere.com/paper/PMC12640846/full.md

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Source: https://tomesphere.com/paper/PMC12640846