Evidence map›Paper›PMID 24498175›Full record

ArticlePloS one2014

Invariant NKT cells regulate the CD8 T cell response during Theiler's virus infection.

Lennart T Mars, Magali Mas, Lucie Beaudoin, Jan Bauer, Maria Leite-de-Moraes, Agnès Lehuen, Jean-Francois Bureau, Roland S Liblau

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. The immune system in neurological diseases: What innate-like T cells have to say.The Journal of allergy and clinical immunology · 2024
    Review
  4. Article
  5. Journal of fungi (Basel, Switzerland) · 2022
    Review
  6. Review
  7. Article
  8. NKT Cells in Neurological Diseases.Frontiers in cellular neuroscience · 2019
    Review
  9. Review
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

8 authors at 8 institutions in 2 countries.

Lennart T MarsInstitut National de la Santé et de la Recherche Médicale (INSERM). Unité Mixte de Recherche (UMR)-1043, Toulouse, France ; Centre National de la Recherche Scientifique (CNRS), UMR 5282, Toulouse, France ; Université de Toulouse, UPS, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse, France.
Magali MasInstitut Cochin, INSERM UMR-1016, CNRS UMR 8104, University Paris-Decartes, Paris, France.
Lucie BeaudoinInstitut Cochin, INSERM UMR-1016, CNRS UMR 8104, University Paris-Decartes, Paris, France.
Jan BauerCenter for Brain Research, Department Neuroimmunology, Medical University of Vienna, Vienna, Austria.
Maria Leite-de-MoraesCNRS-UMR 8147, Université Paris Descartes, Sorbonne Paris Cité, France, Institut Necker Enfants Malades, Paris, France.
Agnès LehuenInstitut Cochin, INSERM UMR-1016, CNRS UMR 8104, University Paris-Decartes, Paris, France.
Jean-Francois BureauUnité Génétique Fonctionnelle des Maladies Infectieuses, Institut Pasteur, Paris, France.
Roland S LiblauInstitut National de la Santé et de la Recherche Médicale (INSERM). Unité Mixte de Recherche (UMR)-1043, Toulouse, France ; Centre National de la Recherche Scientifique (CNRS), UMR 5282, Toulouse, France ; Université de Toulouse, UPS, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse, France.
Centre National de la Recherche Scientifique · FRInserm · FRInstitut Cochin · FRInstitut Pasteur · FRMedical University of Vienna · ATUniversité Fédérale de Toulouse Midi-Pyrénées · FRUniversité Paris Cité · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invariant NKT cells are innate lymphocytes with a broad tissue distribution. Here we demonstrate that iNKT cells reside in the central nervous system (CNS) in the absence of inflammation. Their presence in the CNS dramatically augments following inoculation of C57Bl/6 mice with the neurotropic Theiler's murine encephalomyelitis virus (TMEV). At the peak of inflammation the cellular infiltrate comprises 45,000 iNKT cells for 1250 CD8 T cells specific for the immunodominant TMEV epitope. To study the interaction between these two T cell subsets, we infected both iNKT cell deficient Jα18(-/-) mice and iNKT cell enriched Vα14 transgenic mice with TMEV. The CD8 T cell response readily cleared TMEV infection in the iNKT cell deficient mice. However, in the iNKT cell enriched mice TMEV infection persisted and was associated with significant mortality. This was caused by the inhibition of the CD8 T cell response in the cervical lymph nodes and spleen after T cell priming. Taken together we demonstrate that iNKT cells reside in the CNS in the absence of inflammation and that their enrichment is associated with the inhibition of the anti-viral CD8 T cell response and an augmented mortality during acute encephalomyelitis.

Indexed as

AnimalsCD8-Positive T-LymphocytesCentral Nervous SystemEncephalomyelitisEpitopesInflammationLymph NodesLymphocyte ActivationMiceMice, Inbred C57BLMice, TransgenicNatural Killer T-CellsPoliomyelitisSpleenTheilovirusT-Lymphocyte SubsetsEpitopes

Identifiers

PMID24498175
PMCPMC3907484
OpenAlexW2019755222

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.