Evidence map›Paper›PMID 31815149›Full record

ArticleJournal of immunology research2019

Distinct Redox Signalling following Macrophage Activation Influences Profibrotic Activity.

Caitlin V Lewis, Antony Vinh, Henry Diep, Chrishan S Samuel, Grant R Drummond, Barbara K Kemp-Harper

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

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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 2 institutions in 1 country.

Caitlin V LewisCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.
Antony VinhCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.ORCID https://orcid.org/0000-0001-8367-6134
Henry DiepCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.ORCID https://orcid.org/0000-0001-7818-176X
Chrishan S SamuelCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.ORCID https://orcid.org/0000-0003-0295-4214
Grant R DrummondCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.ORCID https://orcid.org/0000-0001-8556-9738
Barbara K Kemp-HarperCardiovascular Disease Program, Biomedicine Discovery Institute & Department of Pharmacology, Monash University, VIC 3800, Australia.ORCID https://orcid.org/0000-0002-4669-4277
Australian Regenerative Medicine Institute · AULa Trobe University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo date, the ROS-generating capacities of macrophages in different activation states have not been thoroughly compared. This study is aimed at determining the nature and levels of ROS generated following stimulation with common activators of M1 and M2 macrophages and investigating the potential for this to impact fibrosis.

resultsHuman primary and THP-1 macrophages were treated with IFN-

conclusionWe show that superoxide generation is not only enhanced with stimuli associated with M1 macrophage activation but also with the M2 stimulus IL-4. Macrophages activated with IL-4 also exhibited enhanced hydrogen peroxide generation which in turn increased aortic fibroblast collagen production. Thus, M2 macrophage-derived ROS is identified as a potentially important contributor to aortic fibrosis.

Indexed as

CatalaseChemokine CCL22Chemokine CXCL11Chemokines, CCCoculture TechniquesCollagen Type IFibroblastsGene Expression RegulationHumansHydrogen PeroxideInterferon-gammaInterleukin-1betaInterleukin-4LipopolysaccharidesMacrophage ActivationMacrophagesCatalasecatalase-polyethylene glycolCCL18 protein, humanCCL22 protein, humanCCR7 protein, humanChemokine CCL22Chemokine CXCL11Chemokines, CCCollagen Type ICXCL11 protein, humanCYBB protein, humanHydrogen PeroxideIL1B protein, humanIL4 protein, humanInterferon-gammaInterleukin-1betaInterleukin-4LipopolysaccharidesMembrane GlycoproteinsMRC1 protein, humanNADPH Oxidase 2Polyethylene GlycolsReceptors, CCR7Receptors, ImmunologicRNA, Small InterferingSuperoxides

Identifiers

PMID31815149
PMCPMC6877990
OpenAlexW2986181482

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.