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ArticleMolecular neurobiology2026

Comparative Analysis of Mouse CSF Proteins in Experimental Autoimmune Encephalomyelitis Model and Cuprizone-Induced Demyelination Model by Olink Proteomics.

Eline Bernaerts, Marie Rutten, Amber De Visscher, Jarne Beliën, Nele Berghmans, Tania Mitera, Lien De Somer, Patrick Matthys, Jennifer Vandooren

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Eline BernaertsLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.
Marie RuttenNeuro-Immune Connections and Repair (NIC&R) Laboratory, Department of Immunology and Infection, Biomedical Research Institute, Hasselt University, 3590, Diepenbeek, Belgium.
Amber De VisscherLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.
Jarne BeliënLaboratory for Neuroimmunology, Department of Neurosciences, Leuven Brain Institute, KU Leuven, Leuven, Belgium.
Nele BerghmansLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.
Tania MiteraLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.
Lien De SomerDepartment of Pediatrics, University Hospital Leuven, KU Leuven, 3000, Leuven, Belgium.
Patrick MatthysLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium.
Jennifer VandoorenLaboratory of Immunobiology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000, Leuven, Belgium. Jennifer.vandooren@kuleuven.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is marked by an autoimmune-driven inflammatory response within the central nervous system (CNS), resulting in demyelination and associated neurological impairment. To investigate the pathways involved in MS-related neuroinflammation, we performed cerebrospinal fluid (CSF) proteomic profiling (Olink®) across two murine models, i.e., the experimental autoimmune encephalomyelitis (EAE) and the cuprizone (CPZ)-induced demyelination models. Out of the 92 proteins analyzed, five (CCL2, CCL3, EDA2R, Fas, and HGF) were consistently dysregulated in both models, highlighting shared neuroinflammatory features alongside distinct pathological processes. In the EAE model, 31 proteins were upregulated compared to CPZ-intoxicated mice and controls and were mainly related to T cell development, effector functions and migration, reflecting the model's lymphocyte-centric nature. In contrast, the CPZ model showed a downregulation of a single protein, SEZ6L2, when compared to both EAE and controls. These findings emphasize the divergent protein profiles of CSF in EAE and CPZ models and underscore the different inflammatory pathways engaged in distinct pathophysiological mechanisms of MS.

Indexed as

Demyelinating DiseasesEncephalomyelitis, Autoimmune, ExperimentalProteomicsAnimalsCuprizoneDisease Models, AnimalFemaleMiceMice, Inbred C57BLCuprizoneCSF proteinsCuprizone-induced demyelination modelExperimental autoimmune encephalomyelitis model

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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.