Modulation of IRAK4 as a therapeutic strategy against monosodium urate- and xanthine-induced inflammation in macrophages and HepG2 cells

These findings demonstrate the dual anti-inflammatory effect of IRAK4 inhibition in both immune and hepatic cells and suggest a promising strategy to mitigate inflammation in gout.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-01-08
DOI
https://doi.org/10.3389/fimmu.2025.1744393
Citations
2
Primary Topic
Immune Response and Inflammation
Type
article
Field-Weighted Citation Impact
48.87

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article

Modulation of IRAK4 as a therapeutic strategy against monosodium urate- and xanthine-induced inflammation in macrophages and HepG2 cells

Mark Maienschein‐Cline, Sriram Ravindran, Huan T. Chang, Sadiq Umar
2 citations
Frontiers in Immunology
Immune Response and Inflammation
48.87
article

Modulation of IRAK4 as a therapeutic strategy against monosodium urate- and xanthine-induced inflammation in macrophages and HepG2 cells

Mark Maienschein‐Cline, Sriram Ravindran, Huan T. Chang, Sadiq Umar
article en
2 citations

Abstract

These findings demonstrate the dual anti-inflammatory effect of IRAK4 inhibition in both immune and hepatic cells and suggest a promising strategy to mitigate inflammation in gout.

Frontiers in ImmunologyVol. 16
University of Illinois Chicago (US), University of Chicago (US), Jesse Brown VA Medical Center (US)
National Institutes of Health, University of Illinois at Urbana-Champaign
Good health and well-being
Openalex Percentile: Top 0%
Immune Response and Inflammation
48.87
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