Evidence map›Paper›PMID 24920793›Full record

ArticleJournal of virology2014

Intranasal adenovirus-vectored vaccine for induction of long-lasting humoral immunity-mediated broad protection against influenza in mice.

Eun Hye Kim, Hae-Jung Park, Gye-Yeong Han, Man-Ki Song, Alexander Pereboev, Jeong S Hong, Jun Chang, Young-Ho Byun, Baik Lin Seong, Huan H Nguyen

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  3. Single-dose intranasal AdC68-vectored vaccines rapidly protect Syrian hamsters against lethal Nipah virus infection.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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 4 institutions in 2 countries.

Eun Hye KimViral Immunology Laboratory, International Vaccine Institute, Seoul, South Korea.
Hae-Jung ParkViral Immunology Laboratory, International Vaccine Institute, Seoul, South Korea.
Gye-Yeong HanViral Immunology Laboratory, International Vaccine Institute, Seoul, South Korea.
Man-Ki SongViral Immunology Laboratory, International Vaccine Institute, Seoul, South Korea.
Alexander PereboevGene Therapy Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jeong S HongDepartment of Cell Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jun ChangGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, South Korea.
Young-Ho ByunDepartment of Biotechnology and Vaccine Translational Research Center, Yonsei University, Seoul, South Korea.
Baik Lin SeongDepartment of Biotechnology and Vaccine Translational Research Center, Yonsei University, Seoul, South Korea.
Huan H NguyenViral Immunology Laboratory, International Vaccine Institute, Seoul, South Korea hhnguyen@ivi.int.
International Vaccine Institute · KRUniversity of Alabama at Birmingham · USYonsei University · KREwha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledInfluenza vaccines aimed at inducing antibody (Ab) responses against viral surface hemagglutinin (HA) and neuraminidase (NA) provide sterile immunity to infection with the same subtypes. Vaccines targeting viral conserved determinants shared by the influenza A viruses (IAV) offer heterosubtypic immunity (HSI), a broad protection against different subtypes. We proposed that vaccines targeting both HA and the conserved ectodomain of matrix protein 2 (M2e) would provide protection against infection with the same subtype and also HSI against other subtypes. We report here that single intranasal immunization with a recombinant adenovirus (rAd) vector encoding both HA of H5 virus and M2e (rAdH5/M2e) induced significant HA- and M2e-specific Ab responses, along with protection against heterosubtypic challenge in mice. The protection is superior compared to that induced by rAd vector encoding either HA (rAdH5), or M2e (rAdM2e). While protection against homotypic H5 virus is primarily mediated by virus-neutralizing Abs, the cross-protection is associated with Abs directed to conserved stalk HA and M2e that seem to have an additive effect. Consistently, adoptive transfer of antisera induced by rAdH5/M2e provided the best protection against heterosubtypic challenge compared to that provided by antisera derived from mice immunized with rAdH5 or rAdM2e. These results support the development of rAd-vectored vaccines encoding both H5 and M2e as universal vaccines against different IAV subtypes. IMPORTANCE: Current licensed influenza vaccines provide protection limited to the infection with same virus strains; therefore, the composition of influenza vaccines has to be revised every year. We have developed a new universal influenza vaccine that is highly efficient in induction of long-lasting cross-protection against different influenza virus strains. The cross-protection is associated with a high level of vaccine-induced antibodies against the conserved stalk domain of influenza virus hemagglutinin and the ectodomain of matrix protein. The vaccine could be used to stimulate cross-protective antibodies for the prevention and treatment of influenza with immediate effect for individuals who fail to respond to or receive the vaccine in due time. The vaccine offers a new tool to control influenza outbreaks, including pandemics.

Indexed as

Drug CarriersAdenoviridaeAdministration, IntranasalAnimalsAntibodies, ViralCross ProtectionDisease Models, AnimalFemaleGenetic VectorsHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesMice, Inbred BALB COrthomyxoviridaeOrthomyxoviridae InfectionsVaccinationVaccines, SyntheticAntibodies, ViralDrug Carriershemagglutinin, avian influenza A virusHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesM1 protein, Influenza A virusVaccines, SyntheticViral Matrix Proteins

Identifiers

PMID24920793
PMCPMC4136366
OpenAlexW2039667998

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.