Evidence map›Paper›PMID 26022440›Full record

ArticleThe Journal of infectious diseases2015

Stat1-Deficient Mice Are Not an Appropriate Model for Efficacy Testing of Recombinant Vesicular Stomatitis Virus-Based Filovirus Vaccines.

Andrea Marzi, Lisa Kercher, Joshua Marceau, Anthony York, Julie Callsion, Donald J Gardner, Thomas W Geisbert, Heinz Feldmann

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 25% 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, 25 citations in OpenAlex.

  1. Article
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  5. Immunocompromised Cas9 transgenic mice for rapidMolecular therapy. Methods & clinical development · 2021
    Article
  6. Physiopathology and effectiveness of therapeutic vaccines against human papillomavirus.Environmental science and pollution research international · 2021
    Review
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  8. Article
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  11. Review
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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 4 institutions in 1 country.

Andrea MarziLaboratory of Virology.
Lisa KercherRocky Mountain Veterinary Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton.
Joshua MarceauLaboratory of Virology Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula.
Anthony YorkLaboratory of Virology.
Julie CallsionLaboratory of Virology.
Donald J GardnerRocky Mountain Veterinary Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton.
Thomas W GeisbertGalveston National Laboratory Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston.
Heinz FeldmannLaboratory of Virology.
State Key Laboratory of VirologyNational Institutes of Health · USThe University of Texas Medical Branch at Galveston · USUniversity of Montana · US

Funding

Viral Hemorrhagic Fevers: Disease Modeling and TransmissionZIAAI001089 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FELDMANN, HEINRICH · 2009 to 2025
$50.7M
CAP: Trivalent Filovirus Vaccine for Pre- and Post-Exposure VaccinationZIAAI001163 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FELDMANN, HEINRICH · 2012 to 2019
$3.9M
Intramural NIH HHS
6 · The paper itself

Abstract

Stat1(-/-) mice lack a response to interferon α, β, and γ, allowing for replication of nonadapted wild-type (wt) Ebolavirus and Marburgvirus. We sought to establish a mouse model for efficacy testing of live attenuated recombinant vesicular stomatitis virus (rVSV)-based filovirus vaccine vectors using wt Ebolavirus and Marburgvirus challenge strains. While infection of immunocompetent mice with different rVSV-based filovirus vectors did not cause disease, infection of Stat1(-/-) mice with the same vectors resulted in systemic infection and lethal outcome for the majority of tested rVSVs. Despite differences in viral loads, organ tropism was remarkably similar between rVSV filovirus vaccine vectors and rVSVwt, with the exception of the brain. In conclusion, Stat1(-/-) mice are not an appropriate immunocompromised mouse model for efficacy testing of live attenuated, replication-competent rVSV vaccine vectors.

Indexed as

AnimalsChlorocebus aethiopsDisease Models, AnimalEbolavirusFiloviridaeFiloviridae InfectionsGenetic VectorsHemorrhagic Fever, EbolaMarburgvirusMarburg Virus DiseaseMiceSTAT1 Transcription FactorVaccines, AttenuatedVero CellsVesicular StomatitisViral LoadStat1 protein, mouseSTAT1 Transcription FactorVaccines, AttenuatedViral VaccinesEbolavirusMarburgvirusStat1-deficient micevaccineVesicular stomatitis virus

Identifiers

PMID26022440
PMCPMC4564544
OpenAlexW2158342508

What OpenQuestion holds

Textmetadata
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.