Evidence map›Paper›PMID 41987271›Full record

ArticleJournal of neuroinflammation2026

Repetitive trans-spinal magnetic stimulation promotes repair in inflammatory spinal cord injury through sex-dependent immune modulation.

Fannie Semprez, Inès Ziane, Alexandre Du, Inès Istre, Léo Dupuis, Laurine Moncomble, Pauline Neveu, Clémence Raimond, Antoine Fernandes, Jessy Dorange and 2 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Fannie SemprezSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Inès Ziane *Saints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Alexandre Du *Saints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Inès IstreSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Léo DupuisLaboratoire des Maladies Neurodégénératives, Université Paris-Saclay, CEA, CNRS, Fontenay-Aux-Roses, France.
Laurine MoncombleSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Pauline NeveuSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Clémence RaimondSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Antoine FernandesSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Jessy DorangeInstitute for Research and Innovation in Biomedicine (IRIB), Normandie Univ, UNIROUEN, UR3830 GRHVN, Rouen, 76000, France.
Quentin DelarueSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France.
Nicolas GuéroutSaints-Pères Paris Institute for the Neurosciences, Université Paris Cité, CNRS UMR8003, Paris, F-75006, France. nicolas.guerout@u-paris.fr.

Funding

Fondation des Gueules Cassées AP 28-2023, AP 38-2024 and AP 46-2025
6 · The paper itself

Abstract

Spinal cord injuries (SCI), whether traumatic or inflammatory such as transverse myelitis (TM), are characterized by severe neuroinflammation, demyelination, and long-term disabilities. Current treatments remain limited, highlighting the need for novel non-invasive therapeutic approaches. Repetitive magnetic stimulation (RMS) has emerged as a promising strategy, but its mechanisms and efficacy in inflammatory contexts remain poorly described. Here, we investigated the effects of RMS applied as trans-spinal RMS (rTSMS) in a mouse model of focal spinal cord demyelination induced by lysophosphatidylcholine (LPC). When applied one day after LPC injection, rTSMS reduced inflammation, demyelination, and fibroglial scar formation, while promoting early locomotor recovery in both sexes. In contrast, when treatment was initiated three days after LPC injection, corresponding to the peak of motor deficits, rTSMS conferred tissue protection and functional benefits only in female mice. RNA sequencing analyses revealed sex-dependent immune modulation: in females, rTSMS primarily regulated adaptive T cell-related pathways, whereas in males, it mainly targeted innate immune responses such as neutrophil activity and phagocytosis. Complementary in vitro experiments using microglial and macrophage cultures further demonstrated that RMS modulates transcriptomic responses differently depending on cell type and inflammatory state. Specifically, RMS attenuated IL-1-induced pro-inflammatory signaling in macrophages and completely abolished these effects in microglia. Altogether, our findings establish rTSMS as a non-invasive therapy capable of reducing neuroinflammation and demyelination in inflammatory SCI, with pronounced sex-dependent effects. By uncovering distinct immune pathways engaged in male and female mice, this study provides mechanistic insights into rTSMS action and opens perspectives for its translational use in neuroinflammatory diseases.

Indexed as

Magnetic Field TherapyNeuroinflammatory DiseasesSex CharacteristicsSpinal Cord InjuriesAnimalsFemaleInflammationLysophosphatidylcholinesMaleMiceMice, Inbred C57BLMicrogliaLysophosphatidylcholinesDemyelinationImmune modulationRepetitive magnetic StimulationSex differencesSpinal cord injuryTransverse myelitis

Identifiers

PMID41987271
PMCPMC13425870

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.