Evidence map›Paper›PMID 33067651›Full record

ArticleArchives of virology2021

Expression of influenza A virus-derived peptides on a rotavirus VP6-based delivery platform.

Stina Gröhn, Suvi Heinimäki, Kirsi Tamminen, Vesna Blazevic

Abstract read
In one paragraph

Article in Archives of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

4 authors.

Stina GröhnFaculty of Medicine and Health Technology, Vaccine Development and Immunology/Vaccine Research Center, Tampere University, Arvo Ylpön katu 34, FI-33520, Tampere, Finland. stina.grohn@tuni.fi.ORCID http://orcid.org/0000-0002-3772-7233
Suvi Heinimäki *Faculty of Medicine and Health Technology, Vaccine Development and Immunology/Vaccine Research Center, Tampere University, Arvo Ylpön katu 34, FI-33520, Tampere, Finland.
Kirsi Tamminen *Faculty of Medicine and Health Technology, Vaccine Development and Immunology/Vaccine Research Center, Tampere University, Arvo Ylpön katu 34, FI-33520, Tampere, Finland.
Vesna BlazevicFaculty of Medicine and Health Technology, Vaccine Development and Immunology/Vaccine Research Center, Tampere University, Arvo Ylpön katu 34, FI-33520, Tampere, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant protein technology enables the engineering of modern vaccines composed of a carrier protein displaying poorly immunogenic heterologous antigens. One promising carrier is based on the rotavirus inner-capsid VP6 protein. We explored different VP6 insertion sites for the presentation of two peptides (23 and 140 amino acids) derived from the M2 and HA genes of influenza A virus. Both termini and three surface loops of VP6 were successfully exploited as genetic fusion sites, as demonstrated by the expression of the fusion proteins. However, further studies are needed to assess the morphology and immunogenicity of these constructs.

Indexed as

Antibodies, ViralAntibody FormationAntigens, ViralCapsidCapsid ProteinsInfluenza A virusPeptidesRecombinant ProteinsRotavirusAntibodies, ViralAntigens, ViralCapsid ProteinsPeptidesRecombinant ProteinsVP6 protein, Rotavirus

Identifiers

PMID33067651
PMCPMC7567002

What OpenQuestion holds

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Registered trials

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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.