Evidence map›Paper›PMID 26541285›Full record

ArticleJournal of translational medicine2015

Cotton rat immune responses to virus-like particles containing the pre-fusion form of respiratory syncytial virus fusion protein.

Lori McGinnes Cullen, Jorge C G Blanco, Trudy G Morrison

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.7field-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

27 citing papers in PubMed, 34 citations in OpenAlex.

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  14. Comparative models for human nasal infections and immunity.Developmental and comparative immunology · 2019
    Review
  15. Article
  16. Structure-Based Vaccine Antigen Design.Annual review of medicine · 2019
    Review
  17. 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

3 authors at 2 institutions in 1 country.

Lori McGinnes CullenDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, 01655, USA. lori.mcGinnes@umassmed.edu.
Jorge C G BlancoSigmovir Biosystems Inc., Rockville, MD, 20850, USA. j.blanco@sigmovir.com.
Trudy G MorrisonDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, 01655, USA. trudy.morrison@umassmed.edu.
University of Massachusetts Chan Medical School · USSigmovir Biosystems (United States) · US

Funding

Development of VLP vaccine for RSVR42AI109926 · NIAID · SIGMOVIR BIOSYSTEMS, INC. · PI BLANCO, JORGE C · 2016 to 2017
$1.9M
Role of F Protein Conformation in RSV Vaccine EfficacyR56AI114809 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MORRISON, TRUDY G. · 2016 to 2016
$634k
Development of VPL Vaccine for RSVR41AI109926 · NIAID · SIGMOVIR BIOSYSTEMS, INC. · PI BLANCO, JORGE C · 2014 to 2014
$225k
NIAID NIH HHS R41 AI109926NIAID NIH HHS R41AI109926NIAID NIH HHS R42 AI109926NIAID NIH HHS R56 AI114809
6 · The paper itself

Abstract

backgroundVirus-like particles (VLPs) based on Newcastle disease virus (NDV) core proteins, M and NP, and containing two chimera proteins, F/F and H/G, composed of the respiratory syncytial virus (RSV) fusion protein (F) and glycoprotein (G) ectodomains fused to the transmembrane and cytoplasmic domains of the NDV F and HN proteins, respectively, stimulate durable, protective anti-RSV neutralizing antibodies in mice. Furthermore, immunization of mice with a VLP containing a F/F chimera protein with modifications previously reported to stabilize the pre-fusion form of the RSV F protein resulted in significantly improved neutralizing antibody titers over VLPs containing the wild type F protein. The goal of this study was to determine if VLPs containing the pre-fusion form of the RSV F protein stimulated protective immune responses in cotton rats, a more RSV permissive animal model than mice.

methodsCotton rats were immunized intramuscularly with VLPs containing stabilized pre-fusion F/F chimera protein as well as the H/G chimera protein. The anti-RSV F and RSV G antibody responses were determined by ELISA. Neutralizing antibody titers in sera of immunized animals were determined in plaque reduction assays. Protection of the animals from RSV challenge was assessed. The safety of the VLP vaccine was determined by monitoring lung pathology upon RSV challenge of immunized animals.

resultsThe Pre-F/F VLP induced neutralizing titers that were well above minimum levels previously proposed to be required for a successful vaccine and titers significantly higher than those stimulated by RSV infection. In addition, Pre-F/F VLP immunization stimulated higher IgG titers to the soluble pre-fusion F protein than RSV infection. Cotton rats immunized with Pre-F/F VLPs were protected from RSV challenge, and, importantly, the VLP immunization did not result in enhanced respiratory disease upon RSV challenge.

conclusionsVLPs containing the pre-fusion RSV F protein have characteristics required for a safe, effective RSV vaccine.

Indexed as

Respiratory Syncytial VirusesAnimalsAntibodies, NeutralizingAntibodies, ViralBirdsChlorocebus aethiopsCloning, MolecularCOS CellsDisease Models, AnimalElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayFibroblastsHumansImmunizationLungMiceAntibodies, NeutralizingAntibodies, ViralRecombinant Fusion ProteinsVaccines, Virus-Like Particle

Identifiers

PMID26541285
PMCPMC4636065
OpenAlexW2169593550

What OpenQuestion holds

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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.