Evidence map›Paper›PMID 18069096›Full record

ArticleVaccine2008

Immunization with West Nile virus envelope domain III protects mice against lethal infection with homologous and heterologous virus.

Byron E Martina, Penelopie Koraka, Petra van den Doel, Geert van Amerongen, Guus F Rimmelzwaan, Albert D M E Osterhaus

Abstract read
In one paragraph

Article in Vaccine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

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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

6 authors.

Byron E MartinaErasmus Medical Center, Institute of Virology, P.O. Box 1738, 3000 DR Rotterdam, The Netherlands.
Penelopie Koraka
Petra van den Doel
Geert van Amerongen
Guus F Rimmelzwaan
Albert D M E Osterhaus

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Japanese encephalitis virus (JEV) serocomplex-group consists of mosquito-borne flaviviruses, which include West Nile virus (WNV) and JEV, and both may cause severe encephalitis in humans. WNV has spread rapidly across the United States since its introduction in 1999 and its geographical distribution within the western hemisphere is expected to further expand, whereas, JEV is the most common cause of viral encephalitis in Southeast Asia, China and India. Currently, there is no registered human vaccine or specific therapy to prevent or treat WNV infection. Here we describe the efficacy of recombinant domain III (DIII) of WNV glycoprotein E in a mouse model. It induces high neutralizing antibody titers, as well as, protection against lethal WNV infection in C57BL/6 mice. This vaccine preparation also afforded partial protection against lethal JEV infection.

Indexed as

AnimalsAntibodies, ViralBody WeightEncephalitis, JapaneseEncephalitis Virus, JapaneseMiceMice, Inbred C57BLNeutralization TestsSurvival AnalysisVaccines, SubunitVaccines, SyntheticViral Envelope ProteinsWest Nile FeverWest Nile virusWest Nile Virus VaccinesAntibodies, ViralVaccines, SubunitVaccines, SyntheticViral Envelope ProteinsWest Nile Virus Vaccines

Identifiers

PMID18069096
PMCPMC7127062

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.