Evidence map›Paper›PMID 25116127›Full record

ArticlePloS one2014

Second generation inactivated eastern equine encephalitis virus vaccine candidates protect mice against a lethal aerosol challenge.

Shelley P Honnold, Russell R Bakken, Diana Fisher, Cathleen M Lind, Jeffrey W Cohen, Lori T Eccleston, Kevin B Spurgers, Radha K Maheshwari, Pamela J Glass

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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  11. Differential requirements for FcγR engagement by protective antibodies against Ebola virus.Proceedings of the National Academy of Sciences of the United States of America · 2019
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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 2 institutions in 1 country.

Shelley P HonnoldVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America; Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD, United States of America.
Russell R BakkenVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Diana FisherVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Cathleen M LindVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Jeffrey W CohenVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Lori T EcclestonVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Kevin B SpurgersVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
Radha K MaheshwariDepartment of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD, United States of America.
Pamela J GlassVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, United States of America.
United States Army Medical Research Institute of Infectious Diseases · USUniformed Services University of the Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, there are no FDA-licensed vaccines or therapeutics for eastern equine encephalitis virus (EEEV) for human use. We recently developed several methods to inactivate CVEV1219, a chimeric live-attenuated eastern equine encephalitis virus (EEEV). Dosage and schedule studies were conducted to evaluate the immunogenicity and protective efficacy of three potential second-generation inactivated EEEV (iEEEV) vaccine candidates in mice: formalin-inactivated CVEV1219 (fCVEV1219), INA-inactivated CVEV1219 (iCVEV1219) and gamma-irradiated CVEV1219 (gCVEV1219). Both fCVEV1219 and gCVEV1219 provided partial to complete protection against an aerosol challenge when administered by different routes and schedules at various doses, while iCVEV1219 was unable to provide substantial protection against an aerosol challenge by any route, dose, or schedule tested. When evaluating antibody responses, neutralizing antibody, not virus specific IgG or IgA, was the best correlate of protection. The results of these studies suggest that both fCVEV1219 and gCVEV1219 should be evaluated further and considered for advancement as potential second-generation inactivated vaccine candidates for EEEV.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralAzidesEncephalitis Virus, Eastern EquineEncephalomyelitis, EquineFemaleFormaldehydeGamma RaysImmunity, MucosalMiceMice, Inbred BALB CVaccinationVaccines, AttenuatedViral VaccinesAntibodies, NeutralizingAntibodies, ViralAzidesFormaldehydeiodonaphthylazideVaccines, AttenuatedViral Vaccines

Identifiers

PMID25116127
PMCPMC4130539
OpenAlexW1968934525

What OpenQuestion holds

Textmetadata
LicenceCC0
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.