Evidence map›Paper›PMID 38646538›Full record

ArticleFrontiers in immunology2024

Mucosal immunization with a low-energy electron inactivated respiratory syncytial virus vaccine protects mice without Th2 immune bias.

Valentina Eberlein, Sophia Rosencrantz, Julia Finkensieper, Joana Kira Besecke, Yaser Mansuroglu, Jan-Christopher Kamp, Franziska Lange, Jennifer Dressman, Simone Schopf, Christina Hesse and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

14 authors at 6 institutions in 1 country.

Valentina EberleinFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Sophia RosencrantzFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Julia FinkensieperFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Joana Kira BeseckeFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Yaser MansurogluFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Jan-Christopher KampDepartment of Respiratory Medicine and Infectious Diseases, Hannover Medical School, Hannover, Germany.
Franziska LangeFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Jennifer DressmanFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Simone SchopfFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Christina HesseFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Martin ThomaFraunhofer Cluster of Excellence Immune-Mediated Diseases (CIMD), Frankfurt am Main, Germany.
Jasmin FerteyFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Sebastian UlbertFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Thomas GrunwaldFraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Fraunhofer Institute for Cell Therapy and Immunology · DEFraunhofer Institute for Organic Electronics, Electron Beam and Plasma Technology · DEFraunhofer Institute for Translational Medicine and Pharmacology · DEGerman Center for Lung Research · DEFraunhofer Institute for Applied Polymer Research · DEFraunhofer Institute for Manufacturing Engineering and Automation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The respiratory syncytial virus (RSV) is a leading cause of acute lower respiratory tract infections associated with numerous hospitalizations. Recently, intramuscular (i.m.) vaccines against RSV have been approved for elderly and pregnant women. Noninvasive mucosal vaccination, e.g., by inhalation, offers an alternative against respiratory pathogens like RSV. Effective mucosal vaccines induce local immune responses, potentially resulting in the efficient and fast elimination of respiratory viruses after natural infection. To investigate this immune response to an RSV challenge, low-energy electron inactivated RSV (LEEI-RSV) was formulated with phosphatidylcholine-liposomes (PC-LEEI-RSV) or 1,2-dioleoyl-3-trimethylammonium-propane and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DD-LEEI-RSV) for vaccination of mice intranasally. As controls, LEEI-RSV and formalin-inactivated-RSV (FI-RSV) were used

Indexed as

Antibodies, ViralImmunity, MucosalMice, Inbred BALB CRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesTh2 CellsVaccines, InactivatedAnimalsFemaleImmunizationImmunoglobulin AMiceRespiratory Syncytial VirusesRespiratory Syncytial Virus, HumanVaccinationViral LoadAntibodies, ViralImmunoglobulin ARespiratory Syncytial Virus VaccinesVaccines, Inactivatedformulationlow-energy electron irradiation (LEEI)mucosal immunitymucosal vaccinationRespiratory Syncytial Virus (RSV)

Identifiers

PMID38646538
PMCPMC11026718
OpenAlexW4393984048

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.