Evidence map›Paper›PMID 30332405›Full record

ArticlePLoS biology2018

Peripherally derived macrophages modulate microglial function to reduce inflammation after CNS injury.

Andrew D Greenhalgh, Juan G Zarruk, Luke M Healy, Sam J Baskar Jesudasan, Priya Jhelum, Christopher K Salmon, Albert Formanek, Matthew V Russo, Jack P Antel, Dorian B McGavern and 2 more

Abstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing 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

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

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  20. Detrimental influence of Arginase-1 in infiltrating macrophages on poststroke functional recovery and inflammatory milieu.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article

73 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

12 authors.

Andrew D GreenhalghCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.ORCID 0000-0002-4766-2293
Juan G ZarrukCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.
Luke M HealyNeuroimmunology Unit, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Sam J Baskar JesudasanCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.
Priya JhelumCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.
Christopher K SalmonCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.
Albert FormanekCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.
Matthew V RussoViral Immunology and Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America.
Jack P AntelNeuroimmunology Unit, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Dorian B McGavernViral Immunology and Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America.
Barry W McCollUK Dementia Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Samuel DavidCentre for Research in Neuroscience, The Research Institute of the McGill University Health Center, Quebec, Canada.

Funding

Pathogenesis of viral meningitisZIANS003112 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI MCGAVERN, DORIAN · 2009 to 2025
$33.6M
CIHR MOP-14828Medical Research Council MR/L003384/1Medical Research Council MR/R001316/1
6 · The paper itself

Abstract

Infiltrating monocyte-derived macrophages (MDMs) and resident microglia dominate central nervous system (CNS) injury sites. Differential roles for these cell populations after injury are beginning to be uncovered. Here, we show evidence that MDMs and microglia directly communicate with one another and differentially modulate each other's functions. Importantly, microglia-mediated phagocytosis and inflammation are suppressed by infiltrating macrophages. In the context of spinal cord injury (SCI), preventing such communication increases microglial activation and worsens functional recovery. We suggest that macrophages entering the CNS provide a regulatory mechanism that controls acute and long-term microglia-mediated inflammation, which may drive damage in a variety of CNS conditions.

Indexed as

AdultAnimalsCentral Nervous SystemFemaleHealthy VolunteersHumansInflammationLeukocyte CountMacrophagesMaleMiceMice, Inbred C57BLMicrogliaMonocytesPhagocytosisRecovery of Function

Identifiers

PMID30332405
PMCPMC6205650

What OpenQuestion holds

Textmetadata
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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.