Evidence map›Paper›PMID 29629902›Full record

ArticleThe Journal of clinical investigation2018

Humanized mouse model of Rasmussen's encephalitis supports the immune-mediated hypothesis.

Hania Kebir, Lionel Carmant, François Fontaine, Kathie Béland, Ciprian M Bosoi, Nathalie T Sanon, Jorge I Alvarez, Sébastien Desgent, Camille L Pittet, David Hébert and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  8. Review
  9. CNS autoimmune response in the MAM/pilocarpine rat model of epileptogenic cortical malformation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Review
  11. Article
  12. Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  13. Review
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  16. Article
  17. Article
  18. CD8Nature communications · 2019
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 2 countries.

Hania KebirDepartment of Microbiology, Infectious Diseases, and Immunology, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Lionel CarmantCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
François FontaineCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Kathie BélandCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Ciprian M BosoiCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Nathalie T SanonCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Jorge I AlvarezDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sébastien DesgentCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Camille L PittetCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
David HébertCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Marie-Josée LangloisCentre de Recherche du Centre Hospitalier Universitaire Sainte-Justine (CHU Sainte-Justine), Montreal, Quebec, Canada.
Rose-Marie RébillardDepartment of Pediatrics, and.
Dang K NguyenCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Cécile Cieuta-WaltiCentre Hospitalier Universitaire de Sherbrooke, Department of Pediatrics, Université de Sherbrooke, Shebrooke, Quebec, Canada.
Gregory L HolmesDepartment of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
Howard P GoodkinFontaine Research Park, Department of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.
John R MytingerFontaine Research Park, Department of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.
Mary B ConnollyB.C. Children's Hospital, Division of Neurology, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Alexandre PratCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Elie HaddadDepartment of Microbiology, Infectious Diseases, and Immunology, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Centre Hospitalier Universitaire Sainte-Justine · CACentre Hospitalier de l’Université de Montréal · CAUniversity of Virginia · USBC Children's Hospital · CACentre Hospitalier Universitaire de Sherbrooke · CAPediatrics and Genetics · USUniversity of Pennsylvania · USUniversity of Vermont · US

Funding

CIHR 201203MOP-274421
6 · The paper itself

Abstract

Rasmussen's encephalitis (RE) is a chronic inflammatory brain disorder that causes frequent seizures and unilateral hemispheric atrophy with progressive neurological deficits. Hemispherectomy remains the only treatment that leads to seizure freedom for this refractory epileptic syndrome. The absence of an animal model of disease has been a major obstacle hampering the development of effective therapies. Here, we describe an experimental mouse model that shares several clinical and pathological features with the human disease. Immunodeficient mice injected with peripheral blood mononuclear cells from RE patients and monitored by video electroencephalography developed severe seizures of cortical origin and showed intense astrogliosis and accumulation of human IFN-γ- and granzyme B-expressing T lymphocytes in the brain compared with mice injected with immune cells from control subjects. We also provide evidence for the efficacy of α4 integrin blockade, an approved therapy for the treatment of multiple sclerosis and Crohn's disease, in reducing inflammatory markers associated with RE in the CNS. This model holds promise as a valuable tool for understanding the pathology of RE and for developing patient-tailored experimental therapeutics.

Indexed as

AdolescentAdultAnimalsBrainChildDisease Models, AnimalElectroencephalographyEncephalitisFemaleHeterograftsHumansInflammationLeukocytes, MononuclearMaleMiceMiddle AgedImmunologyImmunotherapyMouse modelsNeurological disordersNeuroscience

Identifiers

PMID29629902
PMCPMC5919802
OpenAlexW2796425507

What OpenQuestion holds

Textmetadata
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.