Evidence map›Paper›PMID 22448011›Full record

ArticleThe Journal of infectious diseases2012

A computationally optimized hemagglutinin virus-like particle vaccine elicits broadly reactive antibodies that protect nonhuman primates from H5N1 infection.

Brendan M Giles, Corey J Crevar, Donald M Carter, Stephanie J Bissel, Stacey Schultz-Cherry, Clayton A Wiley, Ted M Ross

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

70 citing papers in PubMed, 118 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 3 countries.

Brendan M GilesCenter for Vaccine Research, University of Pittsburgh, Pennsylvania 15261, USA.
Corey J Crevar
Donald M Carter
Stephanie J Bissel
Stacey Schultz-Cherry
Clayton A Wiley
Ted M Ross
Institut de Recherche Vaccinale · FRUniversity of Pittsburgh · USInstitute of Immunology · HRSt. Jude Children's Research Hospital · US

Funding

Immunology of Infectious DiseaseT32AI060525 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JoAnne L. Flynn · 2005 to 2026
$5.3M
Virus-Like Particle Vaccines for Pandemic InfluenzaU01AI077771 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROSS, TED M · 2008 to 2010
$3.9M
MIDCAREER INVESTIGATOR AWARDK24MH001717 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WILEY, CLAYTON A. · 1999 to 2009
$1.1M
NIAID NIH HHS T32 AI060525NIAID NIH HHS T32AI060525NIAID NIH HHS U01 AI077771NIAID NIH HHS U01AI077771NIMH NIH HHS K24 MH001717NIMH NIH HHS K24MH01717
6 · The paper itself

Abstract

backgroundHighly pathogenic H5N1 avian influenza viruses continue to spread via waterfowl, causing lethal infections in humans. Vaccines can prevent the morbidity and mortality associated with pandemic influenza isolates. Predicting the specific isolate that may emerge from the 10 different H5N1 clades is a tremendous challenge for vaccine design.

methodsIn this study, we generated a synthetic hemagglutinin (HA) on the basis of a new method, computationally optimized broadly reactive antigen (COBRA), which uses worldwide sequencing and surveillance efforts that are specifically focused on sequences from H5N1 clade 2 human isolates.

resultsCynomolgus macaques vaccinated with COBRA clade 2 HA H5N1 virus-like particles (VLPs) had hemagglutination-inhibition antibody titers that recognized a broader number of representative isolates from divergent clades as compared to nonhuman primates vaccinated with clade 2.2 HA VLPs. Furthermore, all vaccinated animals were protected from A/Whooper Swan/Mongolia/244/2005 (WS/05) clade 2.2 challenge, with no virus detected in the nasal or tracheal washes. However, COBRA VLP-vaccinated nonhuman primates had reduced lung inflammation and pathologic effects as compared to those that received WS/05 VLP vaccines.

conclusionsThe COBRA clade 2 HA H5N1 VLP elicits broad humoral immunity against multiple H5N1 isolates from different clades. In addition, the COBRA VLP vaccine is more effective than a homologous vaccine against a highly pathogenic avian influenza virus challenge.

Indexed as

Amino Acid SequenceAnimalsAntibodies, ViralAntigens, ViralCell Line, TransformedComputer-Aided DesignConsensus SequenceDisease Models, AnimalHemagglutinins, ViralHumansInfluenza A Virus, H5N1 SubtypeInfluenza, HumanInfluenza VaccinesLikelihood FunctionsLungMacaca fascicularisAntibodies, ViralAntigens, ViralHemagglutinins, ViralInfluenza VaccinesVaccines, Virus-Like Particle

Identifiers

PMID22448011
PMCPMC3415819
OpenAlexW2153021768

What OpenQuestion holds

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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.