Evidence map›Paper›PMID 22030367›Full record

ArticleClinical and vaccine immunology : CVI2011

Virus-like particle vaccine containing hemagglutinin confers protection against 2009 H1N1 pandemic influenza.

M Jaber Hossain, Melissa Bourgeois, Fu-Shi Quan, Aleksandr S Lipatov, Jae-Min Song, Li-Mei Chen, Richard W Compans, Ian York, Sang-Moo Kang, Ruben O Donis

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.0field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  6. Influence of temperature on the antigenic changes of virus-like particles.Clinical and experimental vaccine research · 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

10 authors at 2 institutions in 1 country.

M Jaber HossainInfluenza Division, Mailstop G-16, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Melissa Bourgeois
Fu-Shi Quan
Aleksandr S Lipatov
Jae-Min Song
Li-Mei Chen
Richard W Compans
Ian York
Sang-Moo Kang
Ruben O Donis
Centers for Disease Control and Prevention · USEmory University · US

Funding

Self-administered microneedle patches for influenza vaccinesU01AI074579 · NIAID · EMORY UNIVERSITY · PI COMPANS, RICHARD W · 2007 to 2011
$7.7M
NIAID NIH HHS AI0680003NIAID NIH HHS AI074579NIAID NIH HHS U01 AI074579
6 · The paper itself

Abstract

Immunization of the world population before an influenza pandemic such as the 2009 H1N1 virus spreads globally is not possible with current vaccine production platforms. New influenza vaccine technologies, such as virus-like-particles (VLPs), offer a promising alternative. Here, we tested the immunogenicity and protective efficacy of a VLP vaccine containing hemagglutinin (HA) and M1 from the 2009 pandemic H1N1 influenza virus (H1N1pdm) in ferrets and compared intramuscular (i.m.) and intranasal (i.n.) routes of immunization. Vaccination of ferrets with VLPs containing the M1 and HA proteins from A/California/04/2009 (H1N1pdm) induced high antibody titers and conferred significant protection against virus challenge. VLP-vaccinated animals lost less weight, shed less virus in nasal washes, and had markedly lower virus titers in all organs tested than naïve controls. A single dose of VLPs, either i.m. or i.n., induced higher levels of antibody than did two doses of commercial split vaccine. Ferrets vaccinated with split vaccine were incompletely protected against challenge; these animals had lower virus titers in olfactory bulbs, tonsils, and intestines, but lost weight and shed virus in nasal washes to a similar extent as naïve controls. Challenge with heterologous A/Brisbane/59/07 (H1N1) virus revealed that the VLPs conferred minimal cross-protection to heterologous infection, as revealed by the lack of reduction in nasal wash and lung virus titers and slightly higher weight loss relative to controls. In summary, these experiments demonstrate the strong immunogenicity and protective efficacy of VLPs compared to the split vaccine and show that i.n. vaccination with VLPs has the potential for highly efficacious vaccination against influenza.

Indexed as

Administration, IntranasalAnimalsAnimal StructuresAntibodies, ViralBody WeightDisease Models, AnimalFerretsHemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesInjections, IntramuscularOrthomyxoviridae InfectionsVaccinationVaccines, VirosomeViral LoadViral Matrix ProteinsAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesM1 protein, Influenza A virusVaccines, VirosomeViral Matrix Proteins

Identifiers

PMID22030367
PMCPMC3232700
OpenAlexW2154423341

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.