Evidence map›Paper›PMID 30333477›Full record

ArticleCell death & disease2018

Inhibiting repulsive guidance molecule-a suppresses secondary progression in mouse models of multiple sclerosis.

Shogo Tanabe, Yuki Fujita, Kaori Ikuma, Toshihide Yamashita

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

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  7. Anti-RGMa neutralizing antibody ameliorates vascular cognitive impairment in mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
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  19. Common Polymorphisms in theFrontiers in cardiovascular medicine · 2021
    Article
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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

4 authors at 2 institutions in 1 country.

Shogo TanabeDepartment of Molecular Neuroscience, World Premier International, Immunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan.
Yuki FujitaDepartment of Molecular Neuroscience, World Premier International, Immunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan.
Kaori IkumaGraduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan.
Toshihide YamashitaDepartment of Molecular Neuroscience, World Premier International, Immunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan. yamashita@molneu.med.osaka-u.ac.jp.ORCID http://orcid.org/0000-0003-4559-7018
Osaka International University · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system that is characterized by motor deficits, fatigue, pain, cognitive impairment, and sensory and visual dysfunction. Secondary progressive multiple sclerosis (SPMS) is a progressive form of MS that develops from relapsing-remitting MS. Repulsive guidance molecule-a (RGMa) has diverse functions, including axon growth inhibition and immune regulation. Here, we show inhibiting RGMa had therapeutic effects in mouse models of SPMS. We induced experimental autoimmune encephalomyelitis in nonobese diabetic mice (NOD-EAE mice) and treated them with humanized anti-RGMa monoclonal antibody. This treatment significantly suppressed secondary progression of disease and inflammation, demyelination and axonal degeneration. In addition, treatment with anti-RGMa antibody promoted the growth of corticospinal tracts and motor recovery in targeted EAE mice with inflammatory lesions in the spinal cord. Collectively, these results show that a humanized anti-RGMa antibody has therapeutic effects in mouse models of SPMS.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedAntigens, CDAnti-Inflammatory AgentsAxonsDemyelinating DiseasesDisease Models, AnimalDisease ProgressionEncephalomyelitis, Autoimmune, ExperimentalFemaleGene Expression RegulationGlial Fibrillary Acidic ProteinGPI-Linked ProteinsLocomotionMiceMice, Inbred NODAntibodies, Monoclonal, HumanizedAntigens, CDAnti-Inflammatory AgentsGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseGPI-Linked ProteinsNerve Tissue ProteinsNeuroprotective AgentsRgma protein, mouse

Identifiers

PMID30333477
PMCPMC6193044
OpenAlexW2896064422

What OpenQuestion holds

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LicenceCC BY
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.