Evidence map›Paper›PMID 32397365›Full record

ReviewCells2020

Macrophage Activation Markers, CD163 and CD206, in Acute-on-Chronic Liver Failure.

Marlene Christina Nielsen, Rasmus Hvidbjerg Gantzel, Joan Clària, Jonel Trebicka, Holger Jon Møller, Henning Grønbæk

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
13.6field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 182 citations in OpenAlex.

  1. Pooled it
  2. The M1/M2 Test System for Determining Macrophage Phenotypes.International journal of molecular sciences · 2026
    Review
  3. Liver Macrophages in the Pathogenesis of Viral Hepatitis.Current issues in molecular biology · 2026
    Review
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36 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 3 countries.

Marlene Christina NielsenDepartment of Clinical Biochemistry, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0003-2008-4224
Rasmus Hvidbjerg GantzelDepartment of Hepatology & Gastroenterology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0002-4589-6539
Joan ClàriaEuropean Foundation for the Study of Chronic Liver Failure (EF-CLIF), 08021 Barcelona, Spain.ORCID 0000-0003-4333-7749
Jonel TrebickaEuropean Foundation for the Study of Chronic Liver Failure (EF-CLIF), 08021 Barcelona, Spain.ORCID 0000-0002-7028-3881
Holger Jon MøllerDepartment of Clinical Biochemistry, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Henning GrønbækDepartment of Hepatology & Gastroenterology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0001-8998-7910
Aarhus University Hospital · DKEuropean Foundation for the Study of Chronic Liver Failure · ESGoethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages facilitate essential homeostatic functions e.g., endocytosis, phagocytosis, and signaling during inflammation, and express a variety of scavenger receptors including CD163 and CD206, which are upregulated in response to inflammation. In healthy individuals, soluble forms of CD163 and CD206 are constitutively shed from macrophages, however, during inflammation pathogen- and damage-associated stimuli induce this shedding. Activation of resident liver macrophages viz. Kupffer cells is part of the inflammatory cascade occurring in acute and chronic liver diseases. We here review the existing literature on sCD163 and sCD206 function and shedding, and potential as biomarkers in acute and chronic liver diseases with a particular focus on Acute-on-Chronic Liver Failure (ACLF). In multiple studies sCD163 and sCD206 are elevated in relation to liver disease severity and established as reliable predictors of morbidity and mortality. However, differences in expression- and shedding-stimuli for CD163 and CD206 may explain dissimilarities in prognostic utility in patients with acute decompensation of cirrhosis and ACLF.

Indexed as

Macrophage ActivationAcute-On-Chronic Liver FailureAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenHumansLectins, C-TypeMacrophagesMannose-Binding LectinsMannose ReceptorReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkersCD163 AntigenLectins, C-TypeMannose-Binding LectinsMannose ReceptorReceptors, Cell SurfaceACLFacute decompensation of cirrhosischronic liver diseaseinflammationliver cirrhosis, acute-on-chronic liver failuremacrophagescavenger receptorsCD163sCD206

Identifiers

PMID32397365
PMCPMC7290463
OpenAlexW3022886767

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.