Evidence map›Paper›PMID 24378714›Full record

ArticleHuman vaccines & immunotherapeutics2014

Single-dose monomeric HA subunit vaccine generates full protection from influenza challenge.

Jyothi K Mallajosyula, Ernie Hiatt, Steve Hume, Ashley Johnson, Trushar Jeevan, Rachel Chikwamba, Gregory P Pogue, Barry Bratcher, Hugh Haydon, Richard J Webby and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  14. Advancements in protein nanoparticle vaccine platforms to combat infectious disease.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2021
    Review
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  17. In Preparation for Outdoor Pharming: Griffithsin Can Be Expressed inFrontiers in bioengineering and biotechnology · 2020
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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

11 authors at 6 institutions in 2 countries.

Jyothi K MallajosyulaTouro University California; Vallejo, CA USA.
Ernie HiattKentucky BioProcessing LLC; Owensboro, KY USA.
Steve HumeKentucky BioProcessing LLC; Owensboro, KY USA.
Ashley JohnsonKentucky BioProcessing LLC; Owensboro, KY USA.
Trushar JeevanSt. Jude Children's Research Hospital; Memphis, TN USA.
Rachel ChikwambaCouncil for Scientific and Industrial Research; Pretoria, South Africa.
Gregory P PogueKentucky BioProcessing LLC; Owensboro, KY USA; IC2 Institute; The University of Texas at Austin; Austin, TX USA.
Barry BratcherKentucky BioProcessing LLC; Owensboro, KY USA.
Hugh HaydonKentucky BioProcessing LLC; Owensboro, KY USA.
Richard J WebbySt. Jude Children's Research Hospital; Memphis, TN USA.
Alison A McCormickTouro University California; Vallejo, CA USA.
Owensboro Health · USTouro University California · USAustin Graduate School of Theology · USCouncil for Scientific and Industrial Research · ZADucks Unlimited · USSt. Jude Children's Research Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant subunit vaccines are an efficient strategy to meet the demands of a possible influenza pandemic, because of rapid and scalable production. However, vaccines made from recombinant hemagglutinin (HA) subunit protein are often of low potency, requiring high dose or boosting to generate a sustained immune response. We have improved the immunogenicity of a plant-made HA vaccine by chemical conjugation to the surface of the Tobacco mosaic virus (TMV) which is non infectious in mammals. We have previously shown that TMV is taken up by mammalian dendritic cells and is a highly effective antigen carrier. In this work, we tested several TMV-HA conjugation chemistries, and compared immunogenicity in mice as measured by anti-HA IgG titers and hemagglutination inhibition (HAI). Importantly, pre-existing immunity to TMV did not reduce initial or boosted titers. Further optimization included dosing with and without alum or oil-in water adjuvants. Surprisingly, we were able to stimulate potent immunogenicity and HAI titers with a single 15 µg dose of HA as a TMV conjugate. We then evaluated the efficacy of the TMV-HA vaccine in a lethal virus challenge in mice. Our results show that a single dose of the TMV-HA conjugate vaccine is sufficient to generate 50% survival, or 100% survival with adjuvant, compared with 10% survival after vaccination with a commercially available H1N1 vaccine. TMV-HA is an effective dose-sparing influenza vaccine, using a single-step process to rapidly generate large quantities of highly effective flu vaccine from an otherwise low potency HA subunit protein.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, ViralDisease Models, AnimalDrug CarriersHemagglutination Inhibition TestsHemagglutinin Glycoproteins, Influenza VirusImmunoglobulin GInfluenza A virusInfluenza VaccinesMice, Inbred BALB COrthomyxoviridae InfectionsSurvival AnalysisTobamovirusVaccinationVaccines, SubunitAdjuvants, ImmunologicAntibodies, ViralDrug CarriersHemagglutinin Glycoproteins, Influenza VirusImmunoglobulin GInfluenza VaccinesVaccines, SubunitVaccines, Syntheticdose sparingH1N1HA subunit proteinInfluenzananoparticleplant made pharmaceuticalsvaccination

Identifiers

PMID24378714
PMCPMC4130260
OpenAlexW2034813530

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.