Evidence map›Paper›PMID 35286211›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

A recombinant VSV-vectored vaccine rapidly protects nonhuman primates against lethal Nipah virus disease.

Stephanie L Foster, Courtney Woolsey, Viktoriya Borisevich, Krystle N Agans, Abhishek N Prasad, Daniel J Deer, Joan B Geisbert, Natalie S Dobias, Karla A Fenton, Robert W Cross and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 64 citations in OpenAlex.

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  17. Nipah virus: a summary for clinicians.International journal of emergency medicine · 2025
    Review
  18. Single-dose intranasal AdC68-vectored vaccines rapidly protect Syrian hamsters against lethal Nipah virus infection.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  19. 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

11 authors at 1 institution in 1 country.

Stephanie L FosterGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0002-3097-1129
Courtney WoolseyGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0003-3389-0137
Viktoriya BorisevichGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.
Krystle N AgansGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0002-7319-6935
Abhishek N PrasadGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0002-4147-2077
Daniel J DeerGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.
Joan B GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.
Natalie S DobiasGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.
Karla A FentonGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0002-5530-6969
Robert W CrossGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0001-7718-1522
Thomas W GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555-0610.ORCID 0000-0003-0858-1877
The University of Texas Medical Branch at Galveston · US

Funding

Regulatory Compliance Core - Galveston National Laboratory BSL4 OperationsUC7AI094660 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Gene Garrard Olinger · 2011 to 2026
$208.8M
DOD | United States Army | U.S. Army Medical Command (MEDCOM) W81XWH1910028NIAID NIH HHS UC7 AI094660U.S. Department of Health and Human Services (HHS) UC7AI094660
6 · The paper itself

Abstract

SignificanceConcern has increased about the pandemic potential of Nipah virus (NiV). Similar to SARS-CoV-2, NiV is an RNA virus that is transmitted by respiratory droplets. There are currently no NiV vaccines licensed for human use. While several preventive vaccines have shown promise in protecting animals against lethal NiV disease, most studies have assessed protection 1 mo after vaccination. However, in order to contain and control outbreaks, vaccines that can rapidly confer protection in days rather than months are needed. Here, we show that a recombinant vesicular stomatitis virus vector expressing the NiV glycoprotein can completely protect monkeys vaccinated 7 d prior to NiV exposure and 67% of animals vaccinated 3 d before NiV challenge.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralBiomarkersGenetic VectorsHenipavirus InfectionsKaplan-Meier EstimateNeutralization TestsNipah VirusOutcome Assessment, Health CarePrimate DiseasesVaccinationVaccines, SyntheticViral LoadViral VaccinesAntibodies, NeutralizingAntibodies, ViralBiomarkersVaccines, SyntheticViral VaccineshenipavirusNipah virusrecombinant vesicular stomatitis virusrVSV-NiVvaccine

Identifiers

PMID35286211
PMCPMC8944267
OpenAlexW4220786646

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.