Evidence map›Paper›PMID 29021612›Full record

ArticleScientific reports2017

IL-15 promotes human myogenesis and mitigates the detrimental effects of TNFα on myotube development.

Mary F O'Leary, Graham R Wallace, Andrew J Bennett, Kostas Tsintzas, Simon W Jones

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

58 citing papers in PubMed, 82 citations in OpenAlex.

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  9. Transient expression of human interleukin-15 inPlant biotechnology (Tokyo, Japan) · 2025
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  13. Vitamin D stimulates Il-15 synthesis in rodent muscle.Biochemistry and biophysics reports · 2025
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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

5 authors at 3 institutions in 1 country.

Mary F O'LearyInstitute of Inflammation and Ageing, MRC-ARUK Centre for Musculoskeletal Ageing Research, University of Birmingham, Birmingham, UK.
Graham R WallaceInstitute of Inflammation and Ageing, MRC-ARUK Centre for Musculoskeletal Ageing Research, University of Birmingham, Birmingham, UK.
Andrew J BennettFRAME Alternatives Laboratory, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, UK.
Kostas TsintzasMRC-ARUK Centre for Musculoskeletal Ageing Research, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, UK. kostas.tsintzas@nottingham.ac.uk.
Simon W JonesInstitute of Inflammation and Ageing, MRC-ARUK Centre for Musculoskeletal Ageing Research, University of Birmingham, Birmingham, UK. s.w.jones@bham.ac.uk.
University of Birmingham · GBFund for the Replacement of Animals in Medical Experiments · GBUniversity of Nottingham · GB

Funding

Medical Research Council MR/K00414X/1Wellcome Trust
6 · The paper itself

Abstract

Studies in murine cell lines and in mouse models suggest that IL-15 promotes myogenesis and may protect against the inflammation-mediated skeletal muscle atrophy which occurs in sarcopenia and cachexia. The effects of IL-15 on human skeletal muscle growth and development remain largely uncharacterised. Myogenic cultures were isolated from the skeletal muscle of young and elderly subjects. Myoblasts were differentiated for 8 d, with or without the addition of recombinant cytokines (rIL-15, rTNFα) and an IL-15 receptor neutralising antibody. Although myotubes were 19% thinner in cultures derived from elderly subjects, rIL-15 increased the thickness of myotubes (MTT) from both age groups to a similar extent. Neutralisation of the high-affinity IL-15 receptor binding subunit, IL-15rα in elderly myotubes confirmed that autocrine concentrations of IL-15 also support myogenesis. Co-incubation of differentiating myoblasts with rIL-15 and rTNFα, limited the reduction in MTT and nuclear fusion index (NFI) associated with rTNFα stimulation alone. IL-15rα neutralisation and rTNFα decreased MTT and NFI further. This, coupled with our observation that myotubes secrete IL-15 in response to TNFα stimulation supports the notion that IL-15 serves to mitigate inflammatory skeletal muscle loss. IL-15 may be an effective therapeutic target for the attenuation of inflammation-mediated skeletal muscle atrophy.

Indexed as

AgedAgingAntibodies, NeutralizingCell DifferentiationCells, CulturedFemaleGene Expression Regulation, DevelopmentalHumansInterleukin-15MaleMuscle DevelopmentMuscle Fibers, SkeletalRecombinant ProteinsTumor Necrosis Factor-alphaAntibodies, NeutralizingInterleukin-15Recombinant ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID29021612
PMCPMC5636823
OpenAlexW2762734331

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.