Evidence map›Paper›PMID 34321090›Full record

ArticleCell & bioscience2021

Persistent deficiency of mucosa-associated invariant T (MAIT) cells during alcohol-related liver disease.

Yujue Zhang, Yuanyuan Fan, Wei He, Yi Han, Huarui Bao, Renjun Yang, Bingbing Wang, Derun Kong, Hua Wang

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Therapeutics for Alcohol-Associated Liver Disease.Annual review of pharmacology and toxicology · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Innate immunity and early liver inflammation.Frontiers in immunology · 2023
    Review
  13. Immune cells in alcohol-related liver disease.Liver research (Beijing, China) · 2022
    Review
  14. Review
  15. Article
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

9 authors at 1 institution in 1 country.

Yujue Zhang *Department of Gastroenterology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Yuanyuan Fan *Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, Anhui, China.
Wei HeSchool of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, Anhui, China.
Yi HanDepartment of Gastroenterology, Fuyang Hospital of Anhui Medical University, Fuyang, 236000, Anhui, P.R. China.
Huarui BaoDepartment of Emergency, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Renjun YangDepartment of Gastroenterology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Bingbing WangDepartment of Gastroenterology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China.
Derun KongDepartment of Gastroenterology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, China. kongderun168@163.com.
Hua WangDepartment of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei, 230032, Anhui, China. wanghua@ahmu.edu.cn.ORCID http://orcid.org/0000-0002-2605-5697
Anhui Medical University · CN

Funding

the Anhui Science and Technology Department: 2018 Key research and development plan projects No.1804h08020260the Research fund project of the Anhui provincial institute of translational medicine No.2017zhyx18
6 · The paper itself

Abstract

backgroundAlcohol-related liver disease (ALD) is a major cause of chronic liver diseases. Inflammatory response is a basic pathological feature of ALD. Mucosal-associated invariant T(MAIT) cells are a novel population of innate immune cells, which may be depleted in various inflammatory diseases. However, the changes of MAIT cell in ALD remains unclear.

resultsIn this study, the levels of MAIT cell were significantly decreased in patients with alcoholic fatty liver disease, alcoholic cirrhosis, and mixed cirrhosis (alcoholic + viral). Furthermore, the reduction of circulating MAIT cells was correlated with liver function in patients with cirrhosis. Functional changes among circulating MAIT cells in patients with alcoholic cirrhosis, including increased production of IL-17A and perforin, and reduced production of TNF-α. Plasma cytokine and chemokine levels were quantified using multiple immunoassays and ELISA. Serum levels of chemokine IL-8 were correlated with MAIT cell frequency in patients with alcoholic cirrhosis. Moreover, no differences were observed in the expression of CCR6, CXCR6, and PD-1 in circulating MAIT cells of patients with alcoholic cirrhosis. The MAIT cells in patients with alcoholic cirrhosis were prone to apoptosis, which was promoted by IL-12, IL-18, and IL-8.

conclusionsOur findings indicate persistent MAIT cell loss during alcohol-related liver disease and suggest that MAIT cells can be promising indicator and therapeutic targets in ALD.

Indexed as

Alcohol-related liver diseaseApoptosisInflammationMucosal-associated invariant T cellsSeverity

Identifiers

PMID34321090
PMCPMC8320031
OpenAlexW3127166027

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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.