Evidence map›Paper›PMID 23988715›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2014

Nanoclusters self-assembled from conformation-stabilized influenza M2e as broadly cross-protective influenza vaccines.

Li Wang, Annie Hess, Timothy Z Chang, Ying-Chun Wang, Julie A Champion, Richard W Compans, Bao-Zhong Wang

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

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  11. Intranasal vaccination with influenza HA/GO-PEI nanoparticles provides immune protection against homo- and heterologous strains.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

7 authors at 2 institutions in 1 country.

Li WangDepartment of Microbiology and Immunology, and Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, USA.
Annie HessGeorgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, GA, USA.
Timothy Z ChangGeorgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, GA, USA.
Ying-Chun WangDepartment of Microbiology and Immunology, and Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, USA.
Julie A ChampionGeorgia Institute of Technology, School of Chemical and Biomolecular Engineering, Atlanta, GA, USA. Electronic address: julie.champion@chbe.gatech.edu.
Richard W CompansDepartment of Microbiology and Immunology, and Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, USA. Electronic address: rcompan@emory.edu.
Bao-Zhong WangDepartment of Microbiology and Immunology, and Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA, USA. Electronic address: bwang3@emory.edu.
Georgia Institute of Technology · USEmory University · US

Funding

Novel Influenza nano vaccines for broad cross protectionR01AI101047 · NIAID · GEORGIA STATE UNIVERSITY · PI WANG, BAOZHONG · 2012 to 2023
$6.1M
Novel VLP vaccines for pandemic influenza virusR01AI068003 · NIAID · EMORY UNIVERSITY · PI COMPANS, RICHARD W · 2006 to 2010
$2.7M
NIAID NIH HHS AI068003NIAID NIH HHS AI101047NIAID NIH HHS R01 AI068003NIAID NIH HHS R01 AI101047
6 · The paper itself

Abstract

Influenza vaccines with broad cross-protection are urgently needed. The highly conserved ectodomain of the influenza matrix protein 2 (M2e) can be a promising candidate if its low immunogenicity was overcome. In this study, we generated protein nanoclusters self-assembled from conformation-stabilized M2e tetramers (tM2e) to improve its immunogenicity. The resulting nanoclusters showed an average hydrodynamic diameter of 227 nm. Vaccination with the nanoclusters by an intranasal route elicited high levels of serum antigen-specific IgG in mice (approximately 100-fold higher than that obtained with soluble tM2e), as well as antigen-specific T cell and mucosal antibody responses. The immunity conferred complete protection against lethal challenge with homo- as well as heterosubtypic viruses. These results demonstrate that nanoclusters assembled from conformation-stabilized M2e are promising as a potential universal influenza A vaccine. Self-assembly into nanoclusters represents a novel approach for increasing the immunogenicity of vaccine antigens. FROM THE CLINICAL EDITOR: In order to develop more effective influenza vaccination, the highly conserved ectodomain of M2e could be a promising candidate. Unfortunately, it is a weak antigen for vaccination purposes. In this study, self-assembled protein nanoclusters of tM2e were generated and tested. The nanoclusters demonstrated superior vaccination properties, with complete protection against lethal challenge in the studied rodent model, raising hope for the introduction of similar vaccines to challenge human influenza outbreaks.

Indexed as

NanoparticlesAmino Acid SequenceAnimalsAntibodies, ViralAntigensAntigens, ViralCpG IslandsImmunoglobulin GInfluenza VaccinesLungMiceMolecular Sequence DataNanotechnologyOrthomyxoviridae InfectionsPeptidesRecombinant ProteinsAntibodies, ViralAntigensAntigens, ViralImmunoglobulin GInfluenza VaccinesM2 protein, Influenza A virusPeptidesRecombinant ProteinsViral Matrix ProteinsViroporin ProteinsCross protectionMatrix protein 2 (M2)Nanocluster

Identifiers

PMID23988715
PMCPMC3948190
OpenAlexW1988654466

What OpenQuestion holds

Textmetadata
LicenceTDM
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.