Evidence map›Paper›PMID 25239488›Full record

ArticleVaccine2014

Investigating the efficacy of monovalent and tetravalent dengue vaccine formulations against DENV-4 challenge in AG129 mice.

Jeremy Fuchs, Haiyan Chu, Peter O'Day, Richard Pyles, Nigel Bourne, Subash C Das, Gregg N Milligan, Alan D T Barrett, Charalambos D Partidos, Jorge E Osorio

Abstract read
In one paragraph

Article in Vaccine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 29 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

10 authors at 3 institutions in 2 countries.

Jeremy FuchsTakeda Vaccines, Inc., Madison, WI, USA.
Haiyan ChuTakeda Vaccines, Inc., Madison, WI, USA.
Peter O'DayTakeda Vaccines, Inc., Madison, WI, USA.
Richard PylesSealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-0436, USA.
Nigel BourneSealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-0436, USA.
Subash C DasTakeda Vaccines, Inc., Madison, WI, USA.
Gregg N MilliganSealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-0436, USA.
Alan D T BarrettSealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555-0436, USA.
Charalambos D PartidosTakeda Vaccines, Inc., Madison, WI, USA. Electronic address: harry.partidos@takeda.com.
Jorge E OsorioTakeda Vaccines, Inc., Madison, WI, USA.
Takeda (Japan) · JPThe University of Texas Medical Branch at Galveston · USTakeda (United States) · US

Funding

Task 7 (C29): Development of a Small Animal Model for Dengue N01AI30065 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · 2007 to 2009
$11.1M
NIAID NIH HHS N01 AI030065NIAID NIH HHS N01 AI 30065
6 · The paper itself

Abstract

Dengue (DEN) is the most important mosquito-borne viral disease, with a major impact on global health and economics, caused by four serologically and distinct viruses termed DENV-1 to DENV-4. Currently, there is no licensed vaccine to prevent DEN. We have developed a live attenuated tetravalent DENV vaccine candidate (TDV) (formally known as DENVax) that has shown promise in preclinical and clinical studies and elicits neutralizing antibody responses to all four DENVs. As these responses are lowest to DENV-4 we have used the AG129 mouse model to investigate the immunogenicity of monovalent TDV-4 or tetravalent TDV vaccines, and their efficacy against lethal DENV-4 challenge. Since the common backbone of TDV is based on an attenuated DENV-2 strain (TDV-2) we also tested the efficacy of TDV-2 against DENV-4 challenge. Single doses of the tetravalent or monovalent vaccines elicited neutralizing antibodies, anti-NS1 antibodies, and cellular responses to both envelope and nonstructural proteins. All vaccinated animals were protected against challenge at 60 days post-immunization, whereas all control animals died. Investigation of DENV-4 viremias post-challenge showed that only the control animals had high viremias on day 3 post-challenge, whereas vaccinated mice had no detectable viremia. Overall, these data highlight the excellent immunogenicity and efficacy profile of our candidate dengue vaccine in AG129 mice.

Indexed as

Antibody FormationAnimalsAntibodies, NeutralizingAntibodies, ViralDengueDengue VaccinesDengue VirusDisease Models, AnimalImmunity, CellularMice, Inbred StrainsT-LymphocytesViremiaAntibodies, NeutralizingAntibodies, ViralDengue VaccinesAG129 miceDengueDengue 4Immune protectionVaccines

Identifiers

PMID25239488
PMCPMC4252871
OpenAlexW2064141152

What OpenQuestion holds

Textmetadata
LicenceTDM
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.