Evidence map›Paper›PMID 28148801›Full record

ArticleJournal of virology2017

Inactivated Recombinant Rabies Viruses Displaying Canine Distemper Virus Glycoproteins Induce Protective Immunity against Both Pathogens.

Renata da Fontoura Budaszewski, Andrew Hudacek, Bevan Sawatsky, Beate Krämer, Xiangping Yin, Matthias J Schnell, Veronika von Messling

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2017. 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
1.9field-weighted citation impact, top 16% 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, 35 citations in OpenAlex.

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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

7 authors at 4 institutions in 3 countries.

Renata da Fontoura BudaszewskiFederal University of Rio Grande do Sul, Porto Alegre, Brazil.
Andrew HudacekDepartment of Microbiology and Immunology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Bevan SawatskyVeterinary Medicine Division, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany.
Beate KrämerVeterinary Medicine Division, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany.
Xiangping YinDepartment of Microbiology and Immunology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Matthias J SchnellDepartment of Microbiology and Immunology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA matthias.schnell@jefferson.edu veronika.vonmessling@pei.de.ORCID http://orcid.org/0000-0001-9040-9405
Veronika von MesslingVeterinary Medicine Division, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany matthias.schnell@jefferson.edu veronika.vonmessling@pei.de.ORCID http://orcid.org/0000-0002-3972-8723
Thomas Jefferson University · USGerman Center for Infection Research · DEPaul Ehrlich Institut · DEUniversidade Federal do Rio Grande do Sul · BR

Funding

Preclinical characterization of a multivalent killed Filovirus/Rabies vaccineR01AI105204 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI SCHNELL, MATTHIAS JOHANNES · 2013 to 2017
$5.0M
A novel vaccine: botulinum neurotoxin subunit on a viral carrier.R42AI073064 · NIAID · MOLECULAR TARGETING TECHNOLOGIES, INC. · PI SCHNELL, MATTHIAS JOHANNES · 2012 to 2014
$2.5M
NIAID NIH HHS R01 AI105204NIAID NIH HHS R42 AI073064
6 · The paper itself

Abstract

The development of multivalent vaccines is an attractive methodology for the simultaneous prevention of several infectious diseases in vulnerable populations. Both canine distemper virus (CDV) and rabies virus (RABV) cause lethal disease in wild and domestic carnivores. While RABV vaccines are inactivated, the live-attenuated CDV vaccines retain residual virulence for highly susceptible wildlife species. In this study, we developed recombinant bivalent vaccine candidates based on recombinant vaccine strain rabies virus particles, which concurrently display the protective CDV and RABV glycoprotein antigens. The recombinant viruses replicated to near-wild-type titers, and the heterologous glycoproteins were efficiently expressed and incorporated in the viral particles. Immunization of ferrets with beta-propiolactone-inactivated recombinant virus particles elicited protective RABV antibody titers, and animals immunized with a combination of CDV attachment protein- and fusion protein-expressing recombinant viruses were protected from lethal CDV challenge. However, animals that were immunized with only a RABV expressing the attachment protein of CDV vaccine strain Onderstepoort succumbed to infection with a more recent wild-type strain, indicating that immune responses to the more conserved fusion protein contribute to protection against heterologous CDV strains.

Indexed as

AnimalsAntibodies, ViralDisease Models, AnimalDistemperDistemper Virus, CanineFerretsRabies virusSurvival AnalysisVaccines, InactivatedVaccines, SyntheticViral VaccinesAntibodies, ViralVaccines, InactivatedVaccines, SyntheticViral Vaccinesantibody responsesbivalent vaccinecanine distemper virusferret modelrabies viruswildlife species

Identifiers

PMID28148801
PMCPMC5375678
OpenAlexW2585072088

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.