Evidence map›Paper›PMID 39944754›Full record

ArticleFrontiers in molecular biosciences2024

Cellular and immune landscape of chronic liver diseases: insights from immunophenotyping.

Shaghayegh Soleimani, Ozgur Albayrak, Kayra Somay, Hong Yang, Buket Yigit, Burge Ulukan, Dila Atak, Murat Akyildiz, Metehan Gursoy, Elif Demirtas and 4 more

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

14 authors.

Shaghayegh Soleimani *Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Türkiye.
Ozgur Albayrak *Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Türkiye.
Kayra Somay *Department of Internal Medicine, School of Medicine, Koç University, Istanbul, Türkiye.
Hong YangScience for Life Laboratory, KTH - Royal Institute of Technology, Stockholm, Sweden.
Buket YigitDepartment of Gastroenterology and Hepatology, School of Medicine, Koç University, Istanbul, Türkiye.
Burge UlukanDepartment of Gastroenterology and Hepatology, School of Medicine, Koç University, Istanbul, Türkiye.
Dila AtakDepartment of Gastroenterology and Hepatology, School of Medicine, Koç University, Istanbul, Türkiye.
Murat AkyildizDepartment of Gastroenterology and Hepatology, School of Medicine, Koç University, Istanbul, Türkiye.
Metehan GursoyDepartment of Internal Medicine, School of Medicine, Koç University, Istanbul, Türkiye.
Elif DemirtasDepartment of Internal Medicine, School of Medicine, Koç University, Istanbul, Türkiye.
Adil MardinogluScience for Life Laboratory, KTH - Royal Institute of Technology, Stockholm, Sweden.
Atay VuralKoç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Türkiye.
Murat DayangacDepartment of General Surgery, Medipol University, Istanbul, Türkiye.
Mujdat ZeybelDepartment of Gastroenterology and Hepatology, School of Medicine, Koç University, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic liver disease due to alcohol-related liver disease and chronic viral hepatitis pose a substantial burden on healthcare systems. Chronic liver disease may predispose to hepatocellular carcinoma, for which therapeutic options are limited. This study aimed to explore the immune cell characteristics of the clinical conditions. Methods: Explant liver samples were collected from 25 patients for bulk RNA sequencing and flow cytometry analysis. Immune cell populations were characterized by flow cytometry from isolated hepatic and peripheral mononuclear cells. Results: Significant differences in immune cell characteristics were observed among patients with three clinical conditions. Viral hepatitis and peri-tumor samples exhibited higher hepatic B cell counts compared to alcohol-related liver disease. Additionally, chronic liver disease patients showed higher levels of CD57 Conclusion: This study contributes to the understanding of immune dynamics in chronic liver disease among different etiologies. B lymphocytes are relatively reduced in alcohol-related liver disease compared to other groups, and T cells exhibit a more differentiated subtype. The peritumor microenvironment in HCC suggests a relatively diminished presence of NK cells and a potential tendency toward increased inhibitory characteristics.

Indexed as

chronic liver diseasefibrosishepatic inflammationhepatitisliver immunophenotyping

Identifiers

PMID39944754
PMCPMC11813787

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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.