Targeted inhibitors of S100A9 alleviate chronic pancreatitis by inhibiting M2 macrophage polarization via the TAOK3-JNK signaling pathway

S100A9 is a significant promoter of M2-like macrophage-induced fibrosis in CP via the TAOK3-JNK signaling pathway. Cobamamide and daptomycin, targeted inhibitors of the S100A9-TAOK3 interaction, may become candidate drugs for CP immunotherapy.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-03-25
DOI
https://doi.org/10.3389/fimmu.2025.1526813
Citations
3
Primary Topic
Pancreatitis Pathology and Treatment
Type
article
Field-Weighted Citation Impact
6.02
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article

Targeted inhibitors of S100A9 alleviate chronic pancreatitis by inhibiting M2 macrophage polarization via the TAOK3-JNK signaling pathway

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3 citations
Frontiers in Immunology
Pancreatitis Pathology and Treatment
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article

Targeted inhibitors of S100A9 alleviate chronic pancreatitis by inhibiting M2 macrophage polarization via the TAOK3-JNK signaling pathway

Deshi Dong, Xufeng Tao, Yu Zhan, Hong Xiang, Fangyue Guo, Yu Wu, Dong Shang, Xiaohan Zhai, Linlin Lv
article en
3 citations

Abstract

S100A9 is a significant promoter of M2-like macrophage-induced fibrosis in CP via the TAOK3-JNK signaling pathway. Cobamamide and daptomycin, targeted inhibitors of the S100A9-TAOK3 interaction, may become candidate drugs for CP immunotherapy.

Frontiers in ImmunologyVol. 16
Dalian Medical University (CN), First Affiliated Hospital of Dalian Medical University (CN)
Good health and well-being
Openalex Percentile: Top 5%
Pancreatitis Pathology and Treatment
6.02
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