Evidence map›Paper›PMID 40377492›Full record

ArticleHepatology communications2025

Antioxidant interventions reduced cytokine-induced pyroptosis of peripheral MAIT cells in patients with HBV-related cirrhosis.

Zheng Xu, Zhe Xu, Xing Fan, Meng-Meng Qu, Hongmin Wang, Jiaying Li, Lingyu Gao, Yan-Mei Jiao, Jijing Shi, Fu-Sheng Wang

Abstract read
In one paragraph

Article in Hepatology communications, 2025. 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
–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

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

10 authors.

Zheng XuDepartment of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, Xinjiang, China.ORCID 0009-0000-3064-0285
Zhe XuSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.ORCID 0000-0002-3338-4229
Xing FanSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Meng-Meng QuSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.ORCID 0000-0001-6158-9443
Hongmin WangSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Jiaying LiSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Lingyu GaoKey Medical Laboratory of Stem Cell Transformation and Application, The First People's Hospital of Zhengzhou, Zhengzhou, Henan, China.
Yan-Mei JiaoSenior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.ORCID 0000-0002-2556-326
Jijing ShiKey Medical Laboratory of Stem Cell Transformation and Application, The First People's Hospital of Zhengzhou, Zhengzhou, Henan, China.
Fu-Sheng WangDepartment of Immunology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, Xinjiang, China.ORCID 0000-0002-8043-6685

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucosal-associated invariant T (MAIT) cells are diminished in various liver diseases, but the underlying mechanism remains unclear. This study aimed to investigate the characteristics and underlying mechanisms of MAIT cell depletion in HBV-related cirrhosis.

methodsPeripheral blood samples were collected from 20 healthy controls and 40 patients with HBV-related cirrhosis, divided into compensated (20) and decompensated (20) liver cirrhosis groups. Flow cytometry, single-cell RNA sequencing (scRNA-seq), multiplex immunofluorescence, and ELISA were used to assess MAIT cell characteristics.

resultsIn patients with HBV-related cirrhosis, MAIT cells were significantly reduced and hyperactivated. The levels of pyroptosis and oxidative stress were elevated, particularly in those with decompensated liver cirrhosis (DLC). As disease severity increased, both pyroptosis and oxidative stress in MAIT cells rose, negatively correlating with MAIT cell frequency. Additionally, MAIT cells from patients with compensated liver cirrhosis (CLC) and DLC had lower levels of interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), granzyme B (GZMB), and CD107a, but higher IL-17A levels. Blocking IL-12 and IL-18 pathways reduced MAIT cell activation and pyroptosis, while antioxidants effectively decreased pyroptosis in vitro.

conclusionsPyroptosis contributes to the decline of MAIT cells in HBV-related cirrhosis, while antioxidants can reduce this process.

Indexed as

AntioxidantsCytokinesHepatitis B, ChronicLiver CirrhosisMucosal-Associated Invariant T CellsPyroptosisAdultCase-Control StudiesFemaleGranzymesHumansInterferon-gammaInterleukin-17MaleMiddle AgedOxidative StressAntioxidantsCytokinesGranzymesInterferon-gammaInterleukin-17Tumor Necrosis Factor-alphaantioxidantcytokines pyroptosisHBV-related cirrhosismucosal-associated invariant T cell

Identifiers

PMID40377492
PMCPMC12088640

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.