Evidence map›Paper›PMID 32168345›Full record

ArticlePloS one2020

Characterization of the immune cell landscape of patients with NAFLD.

Tom Diedrich, Silke Kummer, Antonio Galante, Andreas Drolz, Veronika Schlicker, Ansgar W Lohse, Johannes Kluwe, Johanna Maria Eberhard, Julian Schulze Zur Wiesch

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 76 citations in OpenAlex.

  1. Increased Frequency of Dysfunctional Siglec-7Frontiers in immunology · 2021
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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.

Tom DiedrichMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Silke KummerMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Antonio GalanteMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Andreas DrolzMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Veronika SchlickerMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ansgar W LohseMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Johannes KluweMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Johanna Maria EberhardMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Julian Schulze Zur WieschMedical Department, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5033-1938
Universität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple factors are involved in the pathogenesis of non-alcoholic fatty liver disease (NAFLD), but the exact immunological mechanisms that cause inflammation and fibrosis of the liver remain enigmatic. In this current study, cellular samples of a cohort of NAFLD patients (peripheral blood mononuclear cells (PBMC): n = 27, liver samples: n = 15) and healthy individuals (PBMC: n = 26, liver samples: n = 3) were analyzed using 16-color flow cytometry, and the frequency and phenotype of 23 immune cell subtypes was assessed. PBMC of NAFLD patients showed decreased frequencies of total CD3+, CD8+ T cells, CD56dim NK cells and MAIT cells, but elevated frequencies of CD4+ T cells and Th2 cells compared to healthy controls. Intrahepatic lymphocytes (IHL) of NAFLD patients showed decreased frequencies of total T cells, total CD8+ T cells, Vd2+γδ T cells, and CD56bright NK cells, but elevated frequencies of Vδ2-γδ T cells and CD56dim NK cells compared to healthy controls. The activating receptor NKG2D was significantly less frequently expressed among iNKT cells, total NK cells and CD56dim NK cells of PBMC of NAFLD patients compared to healthy controls. More strikingly, hepatic fibrosis as measured by fibroscan elastography negatively correlated with the intrahepatic frequency of total NK cells (r2 = 0,3737, p = 0,02). Hepatic steatosis as measured by controlled attenuation parameter (CAP) value negatively correlated with the frequency of circulating NKG2D+ iNKT cells (r2 = 0,3365, p = 0,0047). Our data provide an overview of the circulating and intrahepatic immune cell composition of NAFLD patients, and point towards a potential role of NK cells and iNKT cells for the regulation of hepatic fibrosis and steatosis in NAFLD.

Indexed as

AdultBiopsyCD3 ComplexCD56 AntigenCD8-Positive T-LymphocytesElasticity Imaging TechniquesFemaleFlow CytometryHumansImmunophenotypingInflammationKiller Cells, NaturalLeukocytes, MononuclearLiverLiver CirrhosisMaleCD3 ComplexCD56 AntigenKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID32168345
PMCPMC7069622
OpenAlexW3011373710

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.