Evidence map›Paper›PMID 30619308›Full record

ReviewFrontiers in immunology2018

The Role of Monocytes and Macrophages in Acute and Acute-on-Chronic Liver Failure.

Evangelos Triantafyllou, Kevin J Woollard, Mark J W McPhail, Charalambos G Antoniades, Lucia A Possamai

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed, 1 pooled it
9.8field-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

162 citing papers in PubMed, 1 synthesis or guideline pooled it, 277 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Expression of CD38Scientific reports · 2026
    Article
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  13. Review
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  18. Discovery of intrahepatic CD103Experimental & molecular medicine · 2025
    Article
  19. Article
  20. RAC1 as a novel therapeutic target for acute liver failure.JHEP reports : innovation in hepatology · 2025
    Article

102 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

5 authors at 2 institutions in 1 country.

Evangelos TriantafyllouDivision of Integrative Systems Medicine and Digestive Disease, Imperial College London, London, United Kingdom.
Kevin J WoollardDivision of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Mark J W McPhailDepartment of Inflammation Biology, Institute of Liver Studies, King's College London, London, United Kingdom.
Charalambos G AntoniadesDivision of Integrative Systems Medicine and Digestive Disease, Imperial College London, London, United Kingdom.
Lucia A PossamaiDivision of Integrative Systems Medicine and Digestive Disease, Imperial College London, London, United Kingdom.
Imperial College London · GBKing's College London · GB

Funding

Medical Research Council MR/M003159/1
6 · The paper itself

Abstract

Acute and acute-on-chronic liver failure (ALF and ACLF), though distinct clinical entities, are considered syndromes of innate immune dysfunction. Patients with ALF and ACLF display evidence of a pro-inflammatory state with local liver inflammation, features of systemic inflammatory response syndrome (SIRS) and vascular endothelial dysfunction that drive progression to multi-organ failure. In an apparent paradox, these patients are concurrently immunosuppressed, exhibiting acquired immune defects that render them highly susceptible to infections. This paradigm of tissue injury succeeded by immunosuppression is seen in other inflammatory conditions such as sepsis, which share poor outcomes and infective complications that account for high morbidity and mortality. Monocyte and macrophage dysfunction are central to disease progression of ALF and ACLF. Activation of liver-resident macrophages (Kupffer cells) by pathogen and damage associated molecular patterns leads to the recruitment of innate effector cells to the injured liver. Early monocyte infiltration may contribute to local tissue destruction during the propagation phase and results in secretion of pro-inflammatory cytokines that drive SIRS. In the hepatic microenvironment, recruited monocytes mature into macrophages following local reprogramming so as to promote resolution responses in a drive to maintain tissue integrity. Intra-hepatic events may affect circulating monocytes through spill over of soluble mediators and exposure to apoptotic cell debris during passage through the liver. Hence, peripheral monocytes show numerous acquired defects in acute liver failure syndromes that impair their anti-microbial programmes and contribute to enhanced susceptibility to sepsis. This review will highlight the cellular and molecular mechanisms by which monocytes and macrophages contribute to the pathophysiology of ALF and ACLF, considering both hepatic inflammation and systemic immunosuppression. We identify areas for further research and potential targets for immune-based therapies to treat these devastating conditions.

Indexed as

Acute DiseaseAcute-On-Chronic Liver FailureHepatitisHumansLiver FailureMacrophagesModels, ImmunologicalMonocytesSepsisSystemic Inflammatory Response Syndromeacute liver failureacute-on-chronic liver failuredamage-associated molecular patternsimmunosuppressionliver inflammationmacrophagesmonocytespathogen-associated molecular patterns

Identifiers

PMID30619308
PMCPMC6302023
OpenAlexW2904758003

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.