Evidence map›Paper›PMID 32660106›Full record

ArticleVaccines2020

A Yellow Fever Virus 17D Infection and Disease Mouse Model Used to Evaluate a Chimeric Binjari-Yellow Fever Virus Vaccine.

Kexin Yan, Laura J Vet, Bing Tang, Jody Hobson-Peters, Daniel J Rawle, Thuy T Le, Thibaut Larcher, Roy A Hall, Andreas Suhrbier

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Safety concern of recombination between self-amplifying mRNA vaccines and viruses is mitigated in vivo.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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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

9 authors at 3 institutions in 2 countries.

Kexin YanInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane 4029, Australia.
Laura J VetSchool of Chemistry and Molecular Biosciences, University of Queensland, St Lucia 4072, Australia.ORCID 0000-0001-7587-2936
Bing TangInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane 4029, Australia.
Jody Hobson-PetersSchool of Chemistry and Molecular Biosciences, University of Queensland, St Lucia 4072, Australia.ORCID 0000-0003-0139-9829
Daniel J RawleInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane 4029, Australia.ORCID 0000-0001-7248-0101
Thuy T LeInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane 4029, Australia.
Thibaut LarcherInstitut National de Recherche Agronomique, Unité Mixte de Recherche 703, Oniris, Nantes CEDEX 03, France.ORCID 0000-0002-0396-3190
Roy A HallSchool of Chemistry and Molecular Biosciences, University of Queensland, St Lucia 4072, Australia.
Andreas SuhrbierInflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane 4029, Australia.ORCID 0000-0001-8986-9025
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUOniris · FR

Funding

National Health and Medical Research Council APP1178896
6 · The paper itself

Abstract

Despite the availability of an effective, live attenuated yellow fever virus (YFV) vaccine (YFV 17D), this flavivirus still causes up to ≈60,000 deaths annually. A number of new approaches are seeking to address vaccine supply issues and improve safety for the immunocompromised vaccine recipients. Herein we describe an adult female IFNAR-/- mouse model of YFV 17D infection and disease that recapitulates many features of infection and disease in humans. We used this model to evaluate a new YFV vaccine that is based on a recently described chimeric Binjari virus (BinJV) vaccine technology. BinJV is an insect-specific flavivirus and the chimeric YFV vaccine (BinJ/YFV-prME) was generated by replacing the prME genes of BinJV with the prME genes of YFV 17D. Such BinJV chimeras retain their ability to replicate to high titers in C6/36 mosquito cells (allowing vaccine production), but are unable to replicate in vertebrate cells. Vaccination with adjuvanted BinJ/YFV-prME induced neutralizing antibodies and protected mice against infection, weight loss and liver pathology after YFV 17D challenge.

Indexed as

Binjari virusmouse modelvaccineyellow fever virus

Identifiers

PMID32660106
PMCPMC7564786
OpenAlexW3041027532

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.