Evidence map›Paper›PMID 24244595›Full record

ArticlePloS one2013

The specificity of targeted vaccines for APC surface molecules influences the immune response phenotype.

Gunnveig Grødeland, Siri Mjaaland, Gro Tunheim, Agnete B Fredriksen, Bjarne Bogen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 18% 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, 41 citations in OpenAlex.

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  5. Neuraminidase delivered as an APC-targeted DNA vaccine induces protective antibodies against influenza.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
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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

5 authors at 2 institutions in 1 country.

Gunnveig GrødelandInstitute of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway ; K.G. Jebsen Centre for Influenza Vaccine Research, University of Oslo, Oslo, Norway.
Siri Mjaaland
Gro Tunheim
Agnete B Fredriksen
Bjarne Bogen
University of Oslo · NONorwegian Institute of Public Health · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Different diseases require different immune responses for efficient protection. Thus, prophylactic vaccines should prime the immune system for the particular type of response needed for protection against a given infectious agent. We have here tested fusion DNA vaccines which encode proteins that bivalently target influenza hemagglutinins (HA) to different surface molecules on antigen presenting cells (APC). We demonstrate that targeting to MHC class II molecules predominantly induced an antibody/Th2 response, whereas targeting to CCR1/3/5 predominantly induced a CD8(+)/Th1 T cell response. With respect to antibodies, the polarizing effect was even more pronounced upon intramuscular (i.m) delivery as compared to intradermal (i.d.) vaccination. Despite these differences in induced immune responses, both vaccines protected against a viral challenge with influenza H1N1. Substitution of HA with ovalbumin (OVA) demonstrated that polarization of immune responses, as a consequence of APC targeting specificity, could be extended to other antigens. Taken together, the results demonstrate that vaccination can be tailor-made to induce a particular phenotype of adaptive immune responses by specifically targeting different surface molecules on APCs.

Indexed as

Adaptive ImmunityAnimalsAntibodies, ViralAntigen PresentationDendritic CellsFemaleGene ExpressionHemagglutinin Glycoproteins, Influenza VirusHistocompatibility Antigens Class IIInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesInjections, IntradermalInjections, IntramuscularMiceMice, Inbred BALB COrthomyxoviridae InfectionsAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusHistocompatibility Antigens Class IIInfluenza VaccinesOvalbuminReceptors, CCRVaccines, Synthetic

Identifiers

PMID24244595
PMCPMC3823800
OpenAlexW1988975403

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.