Iguratimod improves bleomycin-induced pulmonary inflammation and fibrosis by regulating macrophage polarization through inhibiting the TLR4/NF-κB pathway

In summary, IGU inhibits the activation of macrophages and M1 polarization through inhibiting the TLR4/NF-κB pathway, thereby improving BLM-induced pulmonary inflammation and fibrosis in mice. It is suggested that IGU may be a new therapeutic option for interstitial pulmonary fibrosis.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-03-13
DOI
https://doi.org/10.3389/fimmu.2025.1558903
Citations
2
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
3.04
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article

Iguratimod improves bleomycin-induced pulmonary inflammation and fibrosis by regulating macrophage polarization through inhibiting the TLR4/NF-κB pathway

Huan Xu, Koval' Ma, Tingting Zhuang, Ling Lin et al.
2 citations
Frontiers in Immunology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.04
article

Iguratimod improves bleomycin-induced pulmonary inflammation and fibrosis by regulating macrophage polarization through inhibiting the TLR4/NF-κB pathway

Huan Xu, Koval' Ma, Tingting Zhuang, Ling Lin, Z. Ma
article en
2 citations

Abstract

In summary, IGU inhibits the activation of macrophages and M1 polarization through inhibiting the TLR4/NF-κB pathway, thereby improving BLM-induced pulmonary inflammation and fibrosis in mice. It is suggested that IGU may be a new therapeutic option for interstitial pulmonary fibrosis.

Frontiers in ImmunologyVol. 16
Shantou University (CN), First Affiliated Hospital of Shantou University Medical College (CN), Shantou University Medical College (CN)
Good health and well-being
Openalex Percentile: Top 11%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.04
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