Evidence map›Paper›PMID 39789582›Full record

ArticleArthritis research & therapy2025

Inhibition of macrophage polarization and pyroptosis in collagen-induced arthritis through MSC-exo and ginsenoside Rh2.

Zhongsheng Zhou, Shuhui Wu, Yang Li, Pu Shao, Jinlan Jiang

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. The "Tianyu" Formulation Alleviates Rheumatoid Arthritis by Modulating the NLRP3/Caspase-1/GSDMD-Mediated Pyroptosis Pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Zhongsheng ZhouScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130033, China.
Shuhui WuScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130033, China.
Yang LiScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130033, China.
Pu ShaoDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, China. shaopu@jlu.edu.cn.
Jinlan JiangScientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130033, China. jiangjinlan@jlu.edu.cn.

Funding

Department of Science and Technology of Changchun 21ZGY29Department of Science and Technology of Jilin Province 20230505048ZPHealth Service Capacity Enhancement Program of Jilin Province 2017F014Life Spring AKY Pharmaceuticals 3R2211489430National Natural Science Foundation of China 82172230
6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is a chronic autoimmune disease characterized by joint inflammation, tissue damage, and fibrosis, significantly affecting the quality of life. While there are currently some effective treatments available, they often come with side effects. There is an urgent need to find new treatments that can further improve therapeutic outcomes and reduce side effects.

methodsOur study investigates the role of Mesenchymal Stem Cell exosomes (MSC-exo) combined with Ginsenoside Rh2 (Rh2) in the treatment of RA. We specifically focus on how this combined strategy influences macrophage polarization and pyroptosis. This research utilized a collagen-induced rat arthritis model.

resultsThe study findings reveal that the combination of MSC-exo combined with Rh2 can inhibit the polarization of M1 macrophages, increase the proportion of M2-like macrophages, and suppress M1-like macrophage pyroptosis via the NLRP3/Caspase11/GSDMD-N pathway. In the rat arthritis model, the combination of MSC-exo and Rh2 showed synergistic therapeutic effects.

conclusionThis research contributes to a deeper understanding of RA's pathogenesis and presents new potential targeted therapeutic interventions. The combined application of MSC-exo and Rh2 offers promising insights for future innovative strategies in RA treatment, paving the way for more effective management of this autoimmune disease.

Indexed as

Arthritis, ExperimentalGinsenosidesMacrophagesMesenchymal Stem CellsPyroptosisAnimalsArthritis, RheumatoidExosomesMaleRatsRats, Inbred Lewginsenoside Rh2GinsenosidesCollagen-induced arthritisGinsenoside Rh2M1-like macrophagesM2-like macrophagesMesenchymal stem cell exosomesNLRP3/Caspase11/GSDMD-N pathway

Identifiers

PMID39789582
PMCPMC11714916

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.