Evidence map›Paper›PMID 26901122›Full record

ArticlePloS one2016

A Novel Synthetic TLR-4 Agonist Adjuvant Increases the Protective Response to a Clinical-Stage West Nile Virus Vaccine Antigen in Multiple Formulations.

Neal Van Hoeven, Sharvari Waghmare Joshi, Ghislain Ismael Nana, Angela Bosco-Lauth, Christopher Fox, Richard A Bowen, David E Clements, Timothy Martyak, D Elliot Parks, Susan Baldwin and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 33 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

12 authors at 3 institutions in 1 country.

Neal Van HoevenInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Sharvari Waghmare JoshiInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Ghislain Ismael NanaInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Angela Bosco-LauthColorado State University Department of Biomedical Sciences, Foothills Campus, Fort Collins, CO 80523, United States of America.
Christopher FoxInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Richard A BowenColorado State University Department of Biomedical Sciences, Foothills Campus, Fort Collins, CO 80523, United States of America.
David E ClementsHawaii Biotech Inc. 99-193 Aiea Heights Drive, Aiea, Hawaii 96701, United States of America.
Timothy MartyakHawaii Biotech Inc. 99-193 Aiea Heights Drive, Aiea, Hawaii 96701, United States of America.
D Elliot ParksHawaii Biotech Inc. 99-193 Aiea Heights Drive, Aiea, Hawaii 96701, United States of America.
Susan BaldwinInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Steven G ReedInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Rhea N ColerInfectious Disease Research Institute, 1616 Eastlake Ave E., Seattle, WA 98103, United States of America.
Infectious Disease Research Institute · USHawaii Biotech (United States) · USColorado State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

West Nile virus (WNV) is a mosquito-transmitted member of the Flaviviridae family that has emerged in recent years to become a serious public health threat. Given the sporadic nature of WNV epidemics both temporally and geographically, there is an urgent need for a vaccine that can rapidly provide effective immunity. Protection from WNV infection is correlated with antibodies to the viral envelope (E) protein, which encodes receptor binding and fusion functions. Despite many promising E-protein vaccine candidates, there are currently none licensed for use in humans. This study investigates the ability to improve the immunogenicity and protective capacity of a promising clinical-stage WNV recombinant E-protein vaccine (WN-80E) by combining it with a novel synthetic TLR-4 agonist adjuvant. Using the murine model of WNV disease, we find that inclusion of a TLR-4 agonist in either a stable oil-in-water emulsion (SE) or aluminum hydroxide (Alum) formulation provides both dose and dosage sparing functions, whereby protection can be induced after a single immunization containing only 100 ng of WN-80E. Additionally, we find that inclusion of adjuvant with a single immunization reduced viral titers in sera to levels undetectable by viral plaque assay. The enhanced protection provided by adjuvanted immunization correlated with induction of a Th1 T-cell response and the resultant shaping of the IgG response. These findings suggest that inclusion of a next generation adjuvant may greatly enhance the protective capacity of WNV recombinant subunit vaccines, and establish a baseline for future development.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, ViralDose-Response Relationship, ImmunologicFemaleHumansImmunity, CellularMiceTh1 CellsToll-Like Receptor 4Viral Envelope ProteinsWest Nile FeverWest Nile virusWest Nile Virus VaccinesAdjuvants, ImmunologicAntigens, Viralglycoprotein E, FlavivirusTlr4 protein, mouseToll-Like Receptor 4Viral Envelope ProteinsWest Nile Virus Vaccines

Identifiers

PMID26901122
PMCPMC4762984
OpenAlexW2279632482

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.