Evidence map›Paper›PMID 29973940›Full record

ArticleFrontiers in immunology2018

Activation of the Immune-Metabolic Receptor GPR84 Enhances Inflammation and Phagocytosis in Macrophages.

Carlota Recio, Daniel Lucy, Gareth S D Purvis, Poppy Iveson, Lynda Zeboudj, Asif J Iqbal, Daniel Lin, Chris O'Callaghan, Lucy Davison, Esther Griesbach and 5 more

Open access · goldAbstract read
In one paragraph

Article 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 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

91 citing papers in PubMed, 141 citations in OpenAlex.

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  12. Illuminating proinflammatory myeloid cells with PET tracers targeting GPR84.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Immunometabolic Reprogramming by Black Soldier Fly (Animals : an open access journal from MDPI · 2026
    Review
  14. Metabolite sensing receptors in macrophage reprogramming: from inflammation to resolution.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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31 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

15 authors at 2 institutions in 1 country.

Carlota RecioSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Daniel LucySir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Gareth S D PurvisSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Poppy IvesonSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Lynda ZeboudjSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Asif J IqbalSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Daniel LinNuffield Department of Medicine, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Chris O'CallaghanNuffield Department of Medicine, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Lucy DavisonNuffield Department of Medicine, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Esther GriesbachSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Angela J RussellDepartment of Chemistry, University of Oxford, Oxford, United Kingdom.
Graham M WynneDepartment of Chemistry, University of Oxford, Oxford, United Kingdom.
Lea DibKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
Claudia MonacoKennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom.
David R GreavesSir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
University of Oxford · GBCentre for Human Genetics · GB

Funding

KOMP2-Phase3 Production and Phenotyping by the DTCC Consortium TCP Transfer to UC DavisUM1OD023221 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KC KENT LLOYD · 2016 to 2026
$45.7M
British Heart Foundation PG/11/46/28979British Heart Foundation PG/18/1/33430British Heart Foundation RG/15/10/31485Medical Research Council MR/R007977/1NIH HHS UM1 OD023221
6 · The paper itself

Abstract

GPR84 is a member of the metabolic G protein-coupled receptor family, and its expression has been described predominantly in immune cells. GPR84 activation is involved in the inflammatory response, but the mechanisms by which it modulates inflammation have been incompletely described. In this study, we investigated GPR84 expression, activation, and function in macrophages to establish the role of the receptor during the inflammatory response. We observed that GPR84 expression in murine tissues is increased by endotoxemia, hyperglycemia, and hypercholesterolemia.

Indexed as

GPR84immunometabolisminflammationmacrophagesmetabolic G protein-coupled receptors

Identifiers

PMID29973940
PMCPMC6019444
OpenAlexW2806001235

What OpenQuestion holds

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LicenceCC BY
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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.