Evidence map›Paper›PMID 27549017›Full record

ArticleScientific reports2016

Rabbit hemorrhagic disease virus capsid, a versatile platform for foreign B-cell epitope display inducing protective humoral immune responses.

Noelia Moreno, Ignacio Mena, Iván Angulo, Yolanda Gómez, Elisa Crisci, María Montoya, José R Castón, Esther Blanco, Juan Bárcena

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 19 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

9 authors at 3 institutions in 2 countries.

Noelia MorenoCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Ignacio MenaCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Iván AnguloCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Yolanda GómezCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Elisa CrisciCentre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain.
María MontoyaCentre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain.
José R CastónDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología/CSIC, Cantoblanco, 28049 Madrid, Spain.
Esther BlancoCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Juan BárcenaCentro de Investigación en Sanidad Animal (INIA-CISA), Valdeolmos, 28130 Madrid, Spain.
Centro de Investigación en Sanidad AnimalUniversitat Autònoma de Barcelona · ESCentro Nacional de Biotecnología · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus-like particles (VLPs), comprised of viral structural proteins devoid of genetic material, are tunable nanoparticles that can be chemically or genetically engineered, to be used as platforms for multimeric display of foreign antigens. Here, we report the engineering of chimeric VLPs, derived from rabbit hemorrhagic disease virus (RHDV) for presentation of foreign B-cell antigens to the immune system. The RHDV capsid comprises 180 copies of a single capsid subunit (VP60). To evaluate the ability of chimeric RHDV VLPs to elicit protective humoral responses against foreign antigens, we tested two B-cell epitopes: a novel neutralizing B-cell epitope, derived from feline calicivirus capsid protein, and a well characterized B-cell epitope from the extracellular domain of influenza A virus M2 protein (M2e). We generated sets of chimeric RHDV VLPs by insertion of the foreign B-cell epitopes at three different locations within VP60 protein (which involved different levels of surface accessibility) and in different copy numbers per site. The immunogenic potential of the chimeric VLPs was analyzed in the mouse model. The results presented here indicated that chimeric RHDV VLPs elicit potent protective humoral responses against displayed foreign B-cell epitopes, demonstrated by both, in vitro neutralization and in vivo protection against a lethal challenge.

Indexed as

AnimalsB-LymphocytesCapsidCapsid ProteinsEpitopes, B-LymphocyteFemaleHemorrhagic Disease Virus, RabbitImmunity, HumoralImmunizationMice, Inbred BALB CMice, Inbred C57BLProtein EngineeringRabbitsViral Matrix ProteinsViral Structural ProteinsViroporin ProteinsCapsid ProteinsEpitopes, B-LymphocyteM2 protein, Influenza A virusViral Matrix ProteinsViral Structural ProteinsViroporin Proteins

Identifiers

PMID27549017
PMCPMC4994115
OpenAlexW2507840479

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.