Evidence map›Paper›PMID 29263216›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

The STAT3-IL-10-IL-6 Pathway Is a Novel Regulator of Macrophage Efferocytosis and Phenotypic Conversion in Sterile Liver Injury.

Lara Campana, Philip J Starkey Lewis, Antonella Pellicoro, Rebecca L Aucott, Janet Man, Eoghan O'Duibhir, Sarah E Mok, Sofia Ferreira-Gonzalez, Eilidh Livingstone, Stephen N Greenhalgh and 10 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

65 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  18. Review
  19. Efferocytosis in liver disease.JHEP reports : innovation in hepatology · 2024
    Review
  20. Liver Macrophage Diversity in Health and Disease.Results and problems in cell differentiation · 2024
    Review

5 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

20 authors.

Lara CampanaMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom; Lara.Campana@ed.ac.uk.ORCID 0000-0003-1805-4755
Philip J Starkey LewisMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Antonella PellicoroMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Rebecca L AucottMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Janet ManMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Eoghan O'DuibhirMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Sarah E MokUniversity of Edinburgh, Edinburgh EH16 4SB, United Kingdom.
Sofia Ferreira-GonzalezMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Eilidh LivingstoneMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.ORCID 0000-0002-3599-1567
Stephen N GreenhalghMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Katherine L HullUniversity Hospitals of Leicester, Leicester LE3 9QP, United Kingdom.ORCID 0000-0003-0028-5408
Timothy J KendallMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.ORCID 0000-0002-4174-2786
Douglas VernimmenDevelopmental Biology Division, The Roslin Institute, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.ORCID 0000-0002-1308-9919
Neil C HendersonMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Luke BoulterMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom; and.ORCID 0000-0002-7954-6705
Christopher D GregoryMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.ORCID 0000-0002-7553-0132
Yi FengMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.ORCID 0000-0001-8021-7776
Stephen M AndertonMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Stuart J ForbesMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
John P IredaleMedical Research Council Centre for Inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.

Funding

Medical Research Council G0401643Medical Research Council G0600033Medical Research Council G0800682Medical Research Council G0801924Medical Research Council G0900550Medical Research Council G0901697Medical Research Council G1000868Medical Research Council MC_PC_15041Medical Research Council MR/J003611/1Medical Research Council MR/J010766/1Medical Research Council MR/K017047/1Medical Research Council MR/K026666/1Medical Research Council MR/L012766/1Wellcome Trust 072662Wellcome Trust 207793
6 · The paper itself

Abstract

The disposal of apoptotic bodies by professional phagocytes is crucial to effective inflammation resolution. Our ability to improve the disposal of apoptotic bodies by professional phagocytes is impaired by a limited understanding of the molecular mechanisms that regulate the engulfment and digestion of the efferocytic cargo. Macrophages are professional phagocytes necessary for liver inflammation, fibrosis, and resolution, switching their phenotype from proinflammatory to restorative. Using sterile liver injury models, we show that the STAT3-IL-10-IL-6 axis is a positive regulator of macrophage efferocytosis, survival, and phenotypic conversion, directly linking debris engulfment to tissue repair.

Indexed as

Adoptive TransferAnimalsApoptosisHumansInterleukin-10Interleukin-6LiverLiver CirrhosisMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutNecrosisPhagocytosisRegenerationIL10 protein, mouseInterleukin-10Interleukin-6interleukin-6, mouseStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID29263216
PMCPMC5784823

What OpenQuestion holds

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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.