Evidence map›Paper›PMID 21789184›Full record

ArticlePloS one2011

A novel inactivated intranasal respiratory syncytial virus vaccine promotes viral clearance without Th2 associated vaccine-enhanced disease.

Dennis M Lindell, Susan B Morris, Maria P White, Lara E Kallal, Phillip K Lundy, Tarek Hamouda, James R Baker, Nicholas W Lukacs

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 73 citations in OpenAlex.

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  9. Intranasal delivery of allergen in a nanoemulsion adjuvant inhibits allergen-specific reactions in mouse models of allergic airway disease.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2021
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  12. Current Insights into the Host Immune Response to Respiratory Viral Infections.Advances in experimental medicine and biology · 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

8 authors at 3 institutions in 1 country.

Dennis M LindellCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Washington, United States of America.
Susan B Morris
Maria P White
Lara E Kallal
Phillip K Lundy
Tarek Hamouda
James R Baker
Nicholas W Lukacs
Michigan United · USUniversity of Michigan–Ann Arbor · USSeattle Children's Hospital · US

Funding

The Role of C-C Chemokines in Eosinophil Airway InflammationR01AI036302 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKACS, NICHOLAS W · 2001 to 2018
$5.6M
TLR and Notch Ligand in RSV-induced DiseaseR01AI073876 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKACS, NICHOLAS W · 2008 to 2012
$1.9M
B cell antigen presentation in chronic allergic lung disease (asthma)K22AI077712 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI LINDELL, DENNIS M · 2010 to 2011
$272k
NIAID NIH HHS K22 AI077712NIAID NIH HHS K22AI077712NIAID NIH HHS R01 AI036302NIAID NIH HHS R01AI036302NIAID NIH HHS R01 AI073876NIAID NIH HHS R01AI073876
6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV) is a leading cause of bronchiolitis and pneumonia in young children worldwide, and no vaccine is currently available. Inactivated RSV vaccines tested in the 1960's led to vaccine-enhanced disease upon viral challenge, which has undermined RSV vaccine development. RSV infection is increasingly being recognized as an important pathogen in the elderly, as well as other individuals with compromised pulmonary immunity. A safe and effective inactivated RSV vaccine would be of tremendous therapeutic benefit to many of these populations. PRINCIPAL

findingsIn these preclinical studies, a mouse model was utilized to assess the efficacy of a novel, nanoemulsion-adjuvanted, inactivated mucosal RSV vaccine. Our results demonstrate that NE-RSV immunization induced durable, RSV-specific humoral responses, both systemically and in the lungs. Vaccinated mice exhibited increased protection against subsequent live viral challenge, which was associated with an enhanced Th1/Th17 response. In these studies, NE-RSV vaccinated mice displayed no evidence of Th2 mediated immunopotentiation, as has been previously described for other inactivated RSV vaccines.

conclusionsThese studies indicate that nanoemulsion-based inactivated RSV vaccination can augment viral-specific immunity, decrease mucus production and increase viral clearance, without evidence of Th2 immune mediated pathology.

Indexed as

Administration, IntranasalAnimalsAntibody SpecificityBronchial HyperreactivityCytokinesEmulsionsEosinophiliaImmunityImmunizationLungMiceMice, Inbred BALB CNanoparticlesRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesCytokinesEmulsionsRespiratory Syncytial Virus VaccinesVaccines, Inactivated

Identifiers

PMID21789184
PMCPMC3137595
OpenAlexW2031967641

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.