Evidence map›Paper›PMID 28769107›Full record

ArticleScientific reports2017

Innate Immune Basis for Rift Valley Fever Susceptibility in Mouse Models.

Rashida Lathan, Dominique Simon-Chazottes, Grégory Jouvion, Ophélie Godon, Marie Malissen, Marie Flamand, Pierre Bruhns, Jean-Jacques Panthier

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  10. Potent neutralization of Rift Valley fever virus by human monoclonal antibodies through fusion inhibition.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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 3 institutions in 2 countries.

Rashida LathanDepartment of Developmental & Stem Cell Biology, Unit of Mouse Functional Genetics, Institut Pasteur, F-75015, Paris, France.
Dominique Simon-ChazottesDepartment of Developmental & Stem Cell Biology, Unit of Mouse Functional Genetics, Institut Pasteur, F-75015, Paris, France.
Grégory JouvionDepartment of Infection & Epidemiology, Unit of Human Histopathology and Animal Models, Institut Pasteur, F-75015, Paris, France.
Ophélie GodonDepartment of Immunology, Unit of Antibodies in Therapy & Pathology, Institut Pasteur, F-75015, Paris, France.
Marie MalissenCentre d'Immunologie de Marseille-Luminy, Aix Marseille Université UM2, F-13288, Marseille, France.
Marie FlamandDepartment of Virology, Unit of Structural Virology, Institut Pasteur, F-75015, Paris, France.
Pierre BruhnsDepartment of Immunology, Unit of Antibodies in Therapy & Pathology, Institut Pasteur, F-75015, Paris, France.ORCID 0000-0002-4709-8936
Jean-Jacques PanthierDepartment of Developmental & Stem Cell Biology, Unit of Mouse Functional Genetics, Institut Pasteur, F-75015, Paris, France. jean-jacques.panthier@pasteur.fr.
Centre National de la Recherche Scientifique · FRInserm · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rift Valley fever virus (RVFV) leads to varied clinical manifestations in animals and in humans that range from moderate fever to fatal illness, suggesting that host immune responses are important determinants of the disease severity. We investigated the immune basis for the extreme susceptibility of MBT/Pas mice that die with mild to acute hepatitis by day 3 post-infection compared to more resistant BALB/cByJ mice that survive up to a week longer. Lower levels of neutrophils observed in the bone marrow and blood of infected MBT/Pas mice are unlikely to be causative of increased RVFV susceptibility as constitutive neutropenia in specific mutant mice did not change survival outcome. However, whereas MBT/Pas mice mounted an earlier inflammatory response accompanied by higher amounts of interferon (IFN)-α in the serum compared to BALB/cByJ mice, they failed to prevent high viral antigen load. Several immunological alterations were uncovered in infected MBT/Pas mice compared to BALB/cByJ mice, including low levels of leukocytes that expressed type I IFN receptor subunit 1 (IFNAR1) in the blood, spleen and liver, delayed leukocyte activation and decreased percentage of IFN-γ-producing leukocytes in the blood. These observations are consistent with the complex mode of inheritance of RVFV susceptibility in genetic studies.

Indexed as

Immunity, InnateAnimalsAntigens, ViralDisease Models, AnimalDisease SusceptibilityHepatitis, Viral, AnimalLeukocyte CountLiverMaleMiceMice, Inbred BALB CNeutrophilsRift Valley FeverRift Valley fever virusSpleenAntigens, Viral

Identifiers

PMID28769107
PMCPMC5541133
OpenAlexW2740430116

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.