Evidence map›Paper›PMID 42781928›Full record

ArticleJournal of immunology research2026

Mesenchymal Stem Cells Ameliorate Acute-on-Chronic Liver Failure Associated With Expansion of Immunoregulatory Hepatic NKp46

Jing Xiong, Weizhen Weng, Dengna Lin, Huijuan Cao, Shaoquan Zhang, Junfeng Chen, Jing Zhang, Juan Gao, Ildiko Gyory, Zhiliang Gao and 2 more

Abstract read
In one paragraph

Article in Journal of immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Jing XiongDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.ORCID https://orcid.org/0000-0003-1485-2709
Weizhen WengDepartment of Infectious Disease, The Third People's Hospital of Shenzhen, Shenzhen, China, szdsyy.com.
Dengna LinDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.
Huijuan CaoDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.
Shaoquan ZhangDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.
Junfeng ChenDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.
Jing ZhangDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.ORCID https://orcid.org/0000-0003-0375-7095
Juan GaoDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.ORCID https://orcid.org/0000-0003-1236-2634
Ildiko GyoryDepartment of Molecular and Cell Biology, University of Leicester, Leicester, UK, le.ac.uk.
Zhiliang GaoDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.
Shiqiu XiongDepartment of Molecular and Cell Biology, University of Leicester, Leicester, UK, le.ac.uk.
Bingliang LinDepartment of Infectious Diseases, The Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China.ORCID https://orcid.org/0000-0003-4069-6287

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2022A1515110769National Key Research and Development Program of China 2024YFA1108802National Natural Science Foundation of China 81901940Natural Science Foundation of Guangdong Province 2021A1515010306
6 · The paper itself

Abstract

BACKGROUND AND

aimsHepatitis B virus (HBV)-related acute-on-chronic liver failure (HBV-ACLF) is a life-threatening syndrome characterized by rapid hepatic decompensation and immune dysregulation, with limited treatment options. Mesenchymal stem cells (MSCs) have shown therapeutic potential, but their precise mechanisms-particularly regarding their interaction with hepatic NKp46

methodsPeripheral NK cells were analyzed in ACLF patients receiving MSC infusion or standard therapy. Flow cytometry assessed NK frequency, phenotype, and correlations with survival. Murine ACLF was induced by carbon tetrachloride (CCL

resultsFrequency of peripheral blood NK cells from ACLF patients was upregulated after MSCs infusion, which correlated with liver function recovery. Phenotypic changes included upregulation of NKG2A and downregulation of NKp30 and FasL. MSC infusion effectively rescued ACLF mice and increased NK cell frequency in both blood and liver. Strikingly, NKp46

conclusionsMSC infusion holds significant clinical promise for ACLF patients. In addition to promoting liver regeneration, the immunomodulatory effect of MSCs on hepatic NKp46

Indexed as

Acute-On-Chronic Liver FailureKiller Cells, NaturalLiverMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAdultAnimalsAntigens, LyCell ProliferationCells, CulturedCytokinesDisease Models, AnimalFemaleHumansImmunomodulationMaleAntigens, LyCytokinesNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanacute-on-chronic liver failurebone marrow mesenchymal stem cellGM-CSFnatural killer cell

Identifiers

PMID42781928
PMCPMC13602807

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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.