Evidence map›Paper›PMID 31511382›Full record

ArticleJournal of virology2019

Alternative Virus-Like Particle-Associated Prefusion F Proteins as Maternal Vaccines for Respiratory Syncytial Virus.

Jorge C G Blanco, Lurds R Fernando, Wei Zhang, Arash Kamali, Marina S Boukhvalova, Lori McGinnes-Cullen, Trudy G Morrison

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-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

13 citing papers in PubMed, 15 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

7 authors at 2 institutions in 1 country.

Jorge C G BlancoSigmovir Biosystems Inc., Rockville, Maryland, USA j.blanco@sigmovir.com trudy.morrison@umassmed.edu.
Lurds R FernandoSigmovir Biosystems Inc., Rockville, Maryland, USA.
Wei ZhangSigmovir Biosystems Inc., Rockville, Maryland, USA.
Arash KamaliSigmovir Biosystems Inc., Rockville, Maryland, USA.
Marina S BoukhvalovaSigmovir Biosystems Inc., Rockville, Maryland, USA.
Lori McGinnes-CullenDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Trudy G MorrisonDepartment of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts, USA j.blanco@sigmovir.com trudy.morrison@umassmed.edu.
Sigmovir Biosystems (United States) · USUniversity of Massachusetts Chan Medical School · US

Funding

Development of VLP vaccine for RSVR44AI109926 · NIAID · SIGMOVIR BIOSYSTEMS, INC. · PI BLANCO, JORGE C · 2019 to 2021
$3.5M
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 R42 AI109926NIAID NIH HHS R44 AI109926NIAID NIH HHS R56 AI114809
6 · The paper itself

Abstract

Maternal vaccination may be the most effective and safest approach to the protection of infants from respiratory syncytial virus (RSV) infection, a severe acute lower respiratory tract disease in infants and young children worldwide. We previously compared five different virus-like particle (VLP)-associated, mutation-stabilized prefusion F (pre-F) proteins, including the prototype DS-Cav1 F VLPs. We showed that alternative versions of prefusion F proteins have different conformations and induce different populations of anti-F protein antibodies. Two of these alternative pre-F VLPs, the UC-2 F and UC-3 F VLPs, stimulated in mice higher titers of neutralizing antibodies than DS-Cav1 F VLPs (M. L. Cullen, R. M. Schmidt, M. G. Torres, A. A. Capoferri, et al., Vaccines 7:21-41, 2019, https://doi.org/10.3390/vaccines7010021). Here we describe a comparison of these two pre-F VLPs with DS-Cav1 F VLPs as maternal vaccines in cotton rats and report that UC-3 F VLPs significantly increased the neutralizing antibody (NAb) titers in pregnant dams compared to DS-Cav1 F VLPs. The neutralizing antibody titers in the sera of the offspring of the dams immunized with UC-3 F VLPs were significantly higher than those in the sera of the offspring of dams immunized with DS-Cav1 VLPs. This increase in serum NAb titers translated to a 6- to 40-fold lower virus titer in the lungs of the RSV-challenged offspring of dams immunized with UC-3 F VLPs than in the lungs of the RSV-challenged offspring of dams immunized with DS-Cav1 F VLPs. Importantly, the offspring of UC-3 F VLP-immunized dams showed significant protection from lung pathology and from induction of inflammatory lung cytokine mRNA expression after RSV challenge. Immunization with UC-3 F VLPs also induced durable levels of high-titer neutralizing antibodies in dams.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCell LineCytokinesDisease Models, AnimalFemaleGlycoproteinsHumansImmunizationLungRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesRNA, MessengerSigmodontinaeAntibodies, NeutralizingAntibodies, ViralCytokinesF protein, human respiratory syncytial virusGlycoproteinsRespiratory Syncytial Virus VaccinesRNA, MessengerVaccines, Virus-Like ParticleViral Fusion Proteinsglycoproteinsimmune responsematernal immunizationrespiratory syncytial virusvirus-like particles

Identifiers

PMID31511382
PMCPMC6854499
OpenAlexW2972562829

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.