Evidence map›Paper›PMID 31402611›Full record

ArticleAnnals of clinical and translational neurology2019

Autoimmune encephalomyelitis in NOD mice is not initially a progressive multiple sclerosis model.

David Baker, Erik Nutma, Helen O'Shea, Anne Cooke, Jacqueline M Orian, Sandra Amor

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  3. Article
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  7. Myelin-reactive B cells exacerbate CD4Nature communications · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Biological Sex As a Critical Variable in CD4Antioxidants & redox signaling · 2022
    Review
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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 4 institutions in 3 countries.

David BakerBartsMS, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, United Kingdom.ORCID 0000-0002-8872-8711
Erik NutmaDepartment of Pathology, Amsterdam UMC, Location VUmc, Amsterdam, 1081HV, The Netherlands.
Helen O'SheaDepartment of Pathology, University of Cambridge, Cambridge, CB2 1QP, United Kingdom.
Anne CookeDepartment of Pathology, University of Cambridge, Cambridge, CB2 1QP, United Kingdom.
Jacqueline M OrianLa Trobe Institute of Molecular Sciences La Trobe University, Bundoora, Victoria, 3086, Australia.
Sandra AmorBartsMS, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, United Kingdom.ORCID 0000-0001-6169-9845
Queen Mary University of London · GBUniversity of Cambridge · GBAmsterdam Neuroscience · NLLa Trobe University · AU

Funding

Medical Research CouncilNational Multiple Sclerosis Society RG4132A5/1Stichting MS ResearchWellcome Trust
6 · The paper itself

Abstract

objectiveDespite progress in treating relapsing multiple sclerosis (MS), effective inhibition of nonrelapsing progressive MS is an urgent, unmet, clinical need. Animal models of MS, such as experimental autoimmune encephalomyelitis (EAE), provide valuable tools to examine the mechanisms contributing to disease and may be important for developing rational therapeutic approaches for treatment of progressive MS. It has been suggested that myelin oligodendrocyte glycoprotein (MOG) peptide residues 35-55 (MOG

methodsInduction and monitoring of EAE in NOD mice and literature review.

resultsIt is evident that the NOD mouse model lacks validity as a progressive MS model as the individual course seems to be an asynchronous, relapsing-remitting neurodegenerative disease, characterized by increasingly poor recovery from relapse. The seemingly progressive course seen in group means of clinical score is an artifact of data handling and interpretation.

interpretationAlthough MOG

Indexed as

AnimalsDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalMiceMice, Inbred NODMultiple SclerosisMultiple Sclerosis, Chronic ProgressiveMyelin-Oligodendrocyte GlycoproteinMyelin ProteinsNeurodegenerative DiseasesPeptidesMyelin-Oligodendrocyte GlycoproteinMyelin ProteinsPeptides

Identifiers

PMID31402611
PMCPMC6689692
OpenAlexW2956867628

What OpenQuestion holds

Textmetadata
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.