Evidence map›Paper›PMID 37474155›Full record

ArticleThe Journal of infectious diseases2023

Limited Benefit of Postexposure Prophylaxis With VSV-EBOV in Ebola Virus-Infected Rhesus Macaques.

Trenton Bushmaker, Friederike Feldmann, Jamie Lovaglio, Greg Saturday, Amanda J Griffin, Kyle L O'Donnell, James E Strong, Armand Sprecher, Gary Kobinger, Thomas W Geisbert and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

12 authors at 4 institutions in 3 countries.

Trenton BushmakerLaboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.
Friederike FeldmannRocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
Jamie LovaglioRocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
Greg SaturdayRocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
Amanda J GriffinLaboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.
Kyle L O'DonnellLaboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.
James E StrongSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Armand SprecherMédecins Sans Frontières, Brussels, Belgium.
Gary KobingerGalveston National Laboratory, University of Texas Medical Branch at Galveston, Galveston, Texas.
Thomas W GeisbertGalveston National Laboratory, University of Texas Medical Branch at Galveston, Galveston, Texas.
Andrea MarziLaboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.ORCID 0000-0003-0186-9587
Heinz FeldmannLaboratory of Virology, Rocky Mountain Laboratories, National Institutes of Health, Hamilton, Montana.ORCID 0000-0001-9448-8227
National Institutes of Health · USGalveston College · USMédecins Sans Frontières · BEPublic Health Agency of Canada · CA

Funding

Veterinary Services Core for Infectious Diseases Research- RMLZIGAI001048 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HANLEY, PATRICK · 2009 to 2025
$135.0M
Immunobiology, molecular virology and countermeasures of highly pathogenic virusesZIAAI001254 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MARZI, ANDREA · 2020 to 2025
$16.6M
NHLBI NIH HHSNIH HHS
6 · The paper itself

Abstract

Vesicular stomatitis virus-Ebola virus (VSV-EBOV) vaccine has been successfully used in ring vaccination approaches during EBOV disease outbreaks demonstrating its general benefit in short-term prophylactic vaccination, but actual proof of its benefit in true postexposure prophylaxis (PEP) for humans is missing. Animal studies have indicated PEP efficacy when VSV-EBOV was used within hours of lethal EBOV challenge. Here, we used a lower EBOV challenge dose and a combined intravenous and intramuscular VSV-EBOV administration to improve PEP efficacy in the rhesus macaque model. VSV-EBOV treatment 1 hour after EBOV challenge resulted in delayed disease progression but little benefit in outcome. Thus, we could not confirm previous results indicating questionable benefit of VSV-EBOV for EBOV PEP in a nonhuman primate model.

Indexed as

Ebola VaccinesEbolavirusHemorrhagic Fever, EbolaAnimalsHumansMacaca mulattaVesicular stomatitis Indiana virusVesiculovirusEbola Vaccinesadministration routechallenge doseEbola virusErvebopostexposure prophylaxisrhesus macaqueVSV-EBOV

Identifiers

PMID37474155
PMCPMC10651186
OpenAlexW4384923507

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.