Evidence map›Paper›PMID 26307915›Full record

ArticleHuman vaccines & immunotherapeutics2015

Intranasal nanoemulsion-based inactivated respiratory syncytial virus vaccines protect against viral challenge in cotton rats.

Jessica J O'Konek, Paul E Makidon, Jeffrey J Landers, Zhengyi Cao, Carrie-Anne Malinczak, Jessie Pannu, Jennifer Sun, Vira Bitko, Susan Ciotti, Tarek Hamouda and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Vaccines for COVID-19.Clinical and experimental immunology · 2020
    Review
  13. Mucosal vaccines and technology.Clinical and experimental immunology · 2019
    Review
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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 3 institutions in 1 country.

Jessica J O'Koneka Michigan Nanotechnology Institute for Medicine and Biological Sciences; University of Michigan Medical School ; Ann Arbor , MI USA.
Paul E Makidona Michigan Nanotechnology Institute for Medicine and Biological Sciences; University of Michigan Medical School ; Ann Arbor , MI USA.
Jeffrey J Landersa Michigan Nanotechnology Institute for Medicine and Biological Sciences; University of Michigan Medical School ; Ann Arbor , MI USA.
Zhengyi Caoa Michigan Nanotechnology Institute for Medicine and Biological Sciences; University of Michigan Medical School ; Ann Arbor , MI USA.
Carrie-Anne Malinczakc NanoBio Corporation ; Ann Arbor , MI USA.
Jessie Pannuc NanoBio Corporation ; Ann Arbor , MI USA.
Jennifer Sunc NanoBio Corporation ; Ann Arbor , MI USA.
Vira Bitkoc NanoBio Corporation ; Ann Arbor , MI USA.
Susan Ciottic NanoBio Corporation ; Ann Arbor , MI USA.
Tarek Hamoudac NanoBio Corporation ; Ann Arbor , MI USA.
Zbigniew W Wojcinskid Drug Development Preclinical Services, LLC ; Ann Arbor , MI USA.
Nicholas W Lukacse Department of Pathology ; University of Michigan ; Ann Arbor , MI USA.
Ali Fattomc NanoBio Corporation ; Ann Arbor , MI USA.
James R Bakera Michigan Nanotechnology Institute for Medicine and Biological Sciences; University of Michigan Medical School ; Ann Arbor , MI USA.
Ann Arbor Center for Independent Living · USNanoBio (United States) · USUniversity of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory Syncytial Virus is a leading cause of bronchiolitis and pneumonia in infants, the elderly and individuals with compromised immune systems. Despite decades of research, there is currently no available vaccine for RSV. Our group has previously demonstrated that intranasal immunization of mice with RSV inactivated by and adjuvanted with W805EC nanoemulsion elicits robust humoral and cellular immune responses, resulting in protection against RSV infection. This protection was achieved without the induction of airway hyper-reactivity or a Th2-skewed immune response. The cotton rat Sigmodon hispidus has been used for years as an excellent small animal model of RSV disease. Thus, we extended these rodent studies to the more permissive cotton rat model. Intranasal immunization of the nanoemulsion-adjuvanted RSV vaccines induced high antibody titers and a robust Th1-skewed cellular response. Importantly, vaccination provided sterilizing cross-protective immunity against a heterologous RSV challenge and did not induce marked or severe histological effects or eosinophilia in the lung after viral challenge. Overall, these data demonstrate that nanoemulsion-formulated whole RSV vaccines are both safe and effective for immunization in multiple animal models.

Indexed as

Administration, IntranasalAnimalsAntibodies, NeutralizingAntibodies, ViralBronchiolitisCross ProtectionEmulsionsFemaleLungPneumonia, ViralRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesSigmodontinaeTh1 CellsVaccinationAntibodies, NeutralizingAntibodies, ViralEmulsionsRespiratory Syncytial Virus VaccinesVaccines, InactivatedViral Fusion Proteinsadjuvantimmunogenicityintranasal vaccinationnanoemulsionRSVvaccine

Identifiers

PMID26307915
PMCPMC5054793
OpenAlexW2201227995

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.