Evidence map›Paper›PMID 26467630›Full record

ArticleHuman vaccines & immunotherapeutics2016

Rotavirus capsid VP6 protein acts as an adjuvant in vivo for norovirus virus-like particles in a combination vaccine.

Vesna Blazevic, Maria Malm, Daisuke Arinobu, Suvi Lappalainen, Timo Vesikari

Open access · hybridAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2016. 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
2.9field-weighted citation impact, top 9% 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, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. Article
  5. Review
  6. Review
  7. Rotavirus vaccines: progress and new developments.Expert opinion on biological therapy · 2022
    Review
  8. Review
  9. Article
  10. Current and new rotavirus vaccines.Current opinion in infectious diseases · 2019
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
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

5 authors at 2 institutions in 1 country.

Vesna Blazevica Vaccine Research Center, University of Tampere Medical School , Tampere , Finland.
Maria Malma Vaccine Research Center, University of Tampere Medical School , Tampere , Finland.
Daisuke Arinobub R&D Project Office, UMN Pharma Inc. , Yokohama , Kanagawa , Japan.
Suvi Lappalainena Vaccine Research Center, University of Tampere Medical School , Tampere , Finland.
Timo Vesikaria Vaccine Research Center, University of Tampere Medical School , Tampere , Finland.
Tampere University · FITampere University · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotavirus (RV) and norovirus (NoV) are the 2 leading causes of acute viral gastroenteritis worldwide. We have developed a non-live NoV and RV vaccine candidate consisting of NoV virus-like particles (VLPs) and recombinant polymeric RV VP6 protein produced in baculovirus-insect cell expression system. Both components have been shown to induce strong potentially protective immune responses. As VP6 nanotubes are highly immunogenic, we investigated here a possible adjuvant effect of these structures on NoV-specific immune responses in vivo. BALB/c mice were immunized intramuscularly with a suboptimal dose (0.3 μg) of GII.4 or GI.3 VLPs either alone or in a combination with 10 μg dose of VP6 and induction of NoV-specific antibodies in sera of experimental animals were measured. Blocking assay using human saliva or synthetic histo-blood group antigens was employed to test NoV blocking antibodies. Suboptimal doses of the VLPs alone did not induce substantial anti-NoV antibodies. When co-administered with the VP6, considerable titers of not only type-specific but also cross-reactive IgG antibodies against NoV VLP genotypes not included in the vaccine composition were induced. Most importantly, NoV-specific blocking antibodies, a surrogate for neutralizing antibodies, were generated. Our results show that RV VP6 protein has an in vivo adjuvant effect on NoV-specific antibody responses and support the use of VP6 protein as a part of the NoV-RV combination vaccine, especially when addition of external adjuvants is not desirable.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, ViralAntigens, ViralBaculoviridaeCapsid ProteinsCell LineFemaleGenetic VectorsImmunoglobulin GInjections, IntramuscularInsectaMice, Inbred BALB CVaccines, CombinedVaccines, Virus-Like ParticleViral VaccinesAdjuvants, ImmunologicAntibodies, ViralAntigens, ViralCapsid ProteinsImmunoglobulin GVaccines, CombinedVaccines, Virus-Like ParticleViral VaccinesVP6 protein, Rotavirusadjuvantblocking antibodiesnorovirusrotavirusvaccineVLPVP6

Identifiers

PMID26467630
PMCPMC4964741
OpenAlexW2391397132

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.