Evidence map›Paper›PMID 30279468›Full record

ArticleScientific reports2018

Lymphocyte activation gene 3 (Lag3) expression is increased in prion infections but does not modify disease progression.

Yingjun Liu, Silvia Sorce, Mario Nuvolone, Julie Domange, Adriano Aguzzi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
3.1field-weighted citation impact, top 7% 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, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. New implications for prion diseases therapy and prophylaxis.Frontiers in molecular neuroscience · 2024
    Review
  7. Review
  8. Post-inflammatory administration ofFASEB bioAdvances · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Understanding LAG-3 Signaling.International journal of molecular sciences · 2021
    Review
  15. Neuroinflammation in Prion Disease.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. Targeting Alpha-Synuclein as a Therapy for Parkinson's Disease.Frontiers in molecular neuroscience · 2019
    Review
  20. Observational
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

5 authors at 1 institution in 2 countries.

Yingjun LiuInstitute of Neuropathology, University of Zurich, Schmelzbergstrasse 12, CH-8091, Zurich, Switzerland. yingjun.liu@usz.ch.ORCID http://orcid.org/0000-0003-1543-1965
Silvia SorceInstitute of Neuropathology, University of Zurich, Schmelzbergstrasse 12, CH-8091, Zurich, Switzerland.
Mario NuvoloneInstitute of Neuropathology, University of Zurich, Schmelzbergstrasse 12, CH-8091, Zurich, Switzerland.
Julie DomangeInstitute of Neuropathology, University of Zurich, Schmelzbergstrasse 12, CH-8091, Zurich, Switzerland.
Adriano AguzziInstitute of Neuropathology, University of Zurich, Schmelzbergstrasse 12, CH-8091, Zurich, Switzerland. adriano.aguzzi@usz.ch.
University of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prion diseases, Alzheimer's disease and Parkinson's disease (PD) are fatal degenerative disorders that share common neuropathological and biochemical features, including the aggregation of pathological protein conformers. Lymphocyte activation gene 3 (Lag3, also known as CD223) is a member of the immunoglobulin superfamily of receptors expressed on peripheral immune cells, microglia and neurons, which serves as a receptor for α-synuclein aggregates in PD. Here we examined the possible role of Lag3 in the pathogenesis of prion diseases. Through quantitative real-time PCR and RNA-sequencing, we found that the expression levels of Lag3 were relatively low in the adult mouse brains, yet its expression was increased after prion infection. However, we failed finding significant differences regarding the incubation time, PrP

Indexed as

AnimalsAntigens, CDAstrocytesBrainCyclooxygenase 2Disease ProgressionGene Expression RegulationGlial Fibrillary Acidic ProteinInterleukin-12Interleukin-1betaLymphocyte Activation Gene 3 ProteinLymphocytesMiceMice, KnockoutMicrogliaNeuronsAntigens, CDCyclooxygenase 2Glial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseIL1B protein, mouseInterleukin-12Interleukin-1betaLag3 protein, mouseLymphocyte Activation Gene 3 ProteinNitric Oxide Synthase Type IINos2 protein, mousePrPSc ProteinsPtgs2 protein, mouseRNA, MessengerTgfb1 protein, mouseTransforming Growth Factor beta1Tumor Necrosis Factor-alpha

Identifiers

PMID30279468
PMCPMC6168446
OpenAlexW2894413490

What OpenQuestion holds

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LicenceCC BY
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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.