Evidence map›Paper›PMID 22393386›Full record

ArticlePloS one2012

Lethal Nipah virus infection induces rapid overexpression of CXCL10.

Cyrille Mathieu, Vanessa Guillaume, Amélie Sabine, Kien Chai Ong, Kum Thong Wong, Catherine Legras-Lachuer, Branka Horvat

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  6. Article
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  9. Review
  10. Review
  11. Review
  12. Article
  13. The Immunobiology of Nipah Virus.Microorganisms · 2022
    Review
  14. Review
  15. A recombinant VSV-vectored vaccine rapidly protects nonhuman primates against lethal Nipah virus disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. ReprogrammedMicroorganisms · 2021
    Article
  17. Endothelial Cells in Emerging Viral Infections.Frontiers in cardiovascular medicine · 2021
    Review
  18. Article
  19. 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 2 countries.

Cyrille MathieuInserm U758, Human Virology, Ecole Normale Supérieure de Lyon, IFR128 BioSciences Lyon-Gerland Lyon-Sud, University of Lyon 1, Lyon, France.
Vanessa Guillaume
Amélie Sabine
Kien Chai Ong
Kum Thong Wong
Catherine Legras-Lachuer
Branka Horvat
Université Claude Bernard Lyon 1 · FRUniversity of Malaya · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nipah virus (NiV) is a recently emerged zoonotic Paramyxovirus that causes regular outbreaks in East Asia with mortality rate exceeding 75%. Major cellular targets of NiV infection are endothelial cells and neurons. To better understand virus-host interaction, we analyzed the transcriptome profile of NiV infection in primary human umbilical vein endothelial cells. We further assessed some of the obtained results by in vitro and in vivo methods in a hamster model and in brain samples from NiV-infected patients. We found that NiV infection strongly induces genes involved in interferon response in endothelial cells. Among the top ten upregulated genes, we identified the chemokine CXCL10 (interferon-induced protein 10, IP-10), an important chemoattractant involved in the generation of inflammatory immune response and neurotoxicity. In NiV-infected hamsters, which develop pathology similar to what is seen in humans, expression of CXCL10 mRNA was induced in different organs with kinetics that followed NiV replication. Finally, we showed intense staining for CXCL10 in the brain of patients who succumbed to lethal NiV infection during the outbreak in Malaysia, confirming induction of this chemokine in fatal human infections. This study sheds new light on NiV pathogenesis, indicating the role of CXCL10 during the course of infection and suggests that this chemokine may serve as a potential new marker for lethal NiV encephalitis.

Indexed as

Gene Expression RegulationAnimalsCells, CulturedChemokine CXCL10CricetinaeCricetulusEncephalitisEnzyme-Linked Immunosorbent AssayHenipavirus InfectionsHumansHuman Umbilical Vein Endothelial CellsImmunohistochemistryInflammationInterferonsModels, StatisticalNipah VirusChemokine CXCL10CXCL10 protein, humanInterferonsRNA, Messenger

Identifiers

PMID22393386
PMCPMC3290546
OpenAlexW2083321613

What OpenQuestion holds

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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.