Evidence map›Paper›PMID 30585398›Full record

ArticleJournal of cellular and molecular medicine2019

Granulocytic myeloid-derived suppressor cell population increases with the severity of alcoholic liver disease.

Miaomiao Gao, Ang Huang, Zijian Sun, Ying Sun, Binxia Chang, Ji-Yuan Zhang, Zheng-Sheng Zou

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. 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
0.8field-weighted citation impact, top 26% 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, 22 citations in OpenAlex.

  1. Article
  2. Hepatocellular carcinoma: signaling pathways and therapeutic advances.Signal transduction and targeted therapy · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Immunotherapies for hepatocellular carcinoma.Nature reviews. Clinical oncology · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. [Immune cells role and their new potential therapeutic targets in the pathogenesis of alcoholic liver disease].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Review
  14. Article
  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

7 authors at 2 institutions in 2 countries.

Miaomiao GaoCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.
Ang HuangCenter of Non-Infectious Liver Diseases, Beijing 302 Hospital, Beijing, China.
Zijian SunCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.
Ying SunCenter of Non-Infectious Liver Diseases, Beijing 302 Hospital, Beijing, China.
Binxia ChangCenter of Non-Infectious Liver Diseases, Beijing 302 Hospital, Beijing, China.
Ji-Yuan ZhangTreatment and Research Center for Infectious Diseases, Beijing 302 Hospital, Beijing, China.
Zheng-Sheng ZouCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.ORCID 0000-0002-1778-269X
302 Military Hospital of China · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alcoholic liver disease (ALD) is a progressive liver disease that can cause a series of complications, including cirrhosis, liver failure and hepatocellular carcinoma. Granulocytic myeloid-derived suppressor cell (gMDSC) populations have been observed to expand in various liver diseases and to inhibit innate and adaptive immunity in patients with liver disease. However, the characteristics of gMDSCs in patients with ALD have not been studied. We studied 24 healthy controls (HCs) and 107 patients with ALD and found an accumulation of gMDSCs in the peripheral blood of patients with alcoholic liver cirrhosis (ALC). Furthermore, ALC patients with a poor prognosis displayed a significant increase in peripheral gMDSCs and showed an increased capacity for arginase I production compared to HCs. In contrast, plasma arginase I levels in ALC patients were negatively correlated with total bilirubin and international normalized ratio, two key parameters of liver damage. Importantly, gMDSCs accumulated in the livers of ALC patients, and the frequency of liver gMDSCs significantly correlated with that of peripheral gMDSCs. In addition, gMDSC enrichment in vitro significantly inhibited the function of natural killer (NK) cells, perhaps preventing the NK-induced apoptosis of hepatic stellate cells. In summary, increased peripheral and intrahepatic gMDSC populations are present in patients with ALC and may contribute to enhancing the severity of liver cirrhosis.

Indexed as

AdultAgedAged, 80 and overApoptosisCarcinoma, HepatocellularFemaleGranulocytesHepatic Stellate CellsHumansKiller Cells, NaturalLiverLiver Diseases, AlcoholicLiver NeoplasmsMaleMiddle AgedMyeloid-Derived Suppressor Cellsalcoholic liver diseasearginasemyeloid-derived suppressor cellsseverity

Identifiers

PMID30585398
PMCPMC6378203
OpenAlexW2905815518

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.