Evidence map›Paper›PMID 28088249›Full record

ArticleVirology journal2017

Interactions of human microglia cells with Japanese encephalitis virus.

Nils Lannes, Viviane Neuhaus, Brigitte Scolari, Solange Kharoubi-Hess, Michael Walch, Artur Summerfield, Luis Filgueira

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  5. Article
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  7. Article
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  17. Article
  18. Article
  19. Japanese Encephalitis Virus-Infected Cells.Sub-cellular biochemistry · 2023
    Article
  20. 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

7 authors at 2 institutions in 1 country.

Nils LannesDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland. nils.lannes@unifr.ch.
Viviane NeuhausDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland.
Brigitte ScolariDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland.
Solange Kharoubi-HessDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland.
Michael WalchDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland.
Artur SummerfieldInstitute of Virology and Immunology, Sensemattstrasse 293, Mittelhäusern, Switzerland.
Luis FilgueiraDepartment of Medicine, Unit of Anatomy, University of Fribourg, Route Albert-Gockel 1, Fribourg, Switzerland.
University of Fribourg · CHUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundJapanese encephalitis virus (JEV) is a neurotropic flavivirus causing mortality and morbidity in humans. Severe Japanese encephalitis cases display strong inflammatory responses in the central nervous system and an accumulation of viral particles in specific brain regions. Microglia cells are the unique brain-resident immune cell population with potent migratory functions and have been proposed to act as a viral reservoir for JEV. Animal models suggest that the targeting of microglia by JEV is partially responsible for inflammatory reactions in the brain. Nevertheless, the interactions between human microglia and JEV are poorly documented.

methodsUsing human primary microglia and a new model of human blood monocyte-derived microglia, the present study explores the interaction between human microglia and JEV as well as the role of these cells in viral transmission to susceptible cells. To achieve this work, vaccine-containing inactivated JEV and two live JEV strains were applied on human microglia.

resultsLive JEV was non-cytopathogenic to human microglia but increased levels of CCL2, CXCL9 and CXCL10 in such cultures. Furthermore, human microglia up-regulated the expression of the fraktalkine receptor CX

conclusionOur findings suggest that human microglia may be a source of neuronal infection and sustain JEV brain pathogenesis.

Indexed as

Host-Pathogen InteractionsVirus ReplicationCells, CulturedChemokinesEncephalitis Virus, JapaneseHumansMicrogliaChemokinesChemokine ligand-receptorHuman microgliaInflammationJapanese encephalitis virusViral transmission

Identifiers

PMID28088249
PMCPMC5237516
OpenAlexW2574347606

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.