Evidence map›Paper›PMID 29631174›Full record

ArticleVirology2018

Recombinant Flag-tagged E1E2 glycoproteins from three hepatitis C virus genotypes are biologically functional and elicit cross-reactive neutralizing antibodies in mice.

Vasil B Krapchev, Malgorzata Rychłowska, Alicja Chmielewska, Karolina Zimmer, Arvind H Patel, Krystyna Bieńkowska-Szewczyk

Open access · hybridAbstract read
In one paragraph

Article in Virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Challenges and Promise of a Hepatitis C Virus Vaccine.Cold Spring Harbor perspectives in medicine · 2020
    Review
  12. 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

6 authors at 2 institutions in 2 countries.

Vasil B KrapchevLaboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland.
Malgorzata RychłowskaLaboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland.
Alicja ChmielewskaLaboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland.
Karolina ZimmerLaboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland.
Arvind H PatelMRC-University of Glasgow Centre for Virus Research, Sir Michael Stoker Building, Garscube Campus, 464 Bearsden Road, Glasgow G61 1QH, Scotland (UK).
Krystyna Bieńkowska-SzewczykLaboratory of Virus Molecular Biology, Intercollegiate Faculty of Biotechnology of UG and MUG, University of Gdansk, 58 Abrahama str., 80-307 Gdansk, Poland. Electronic address: krystyna.bienkowska-szewczyk@biotech.ug.edu.pl.
University of Gdańsk · PLMRC University of Glasgow Centre for Virus Research · GB

Funding

Medical Research Council MC_U130184144Medical Research Council MC_UU_12014/2
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is a globally disseminated human pathogen for which no vaccine is currently available. HCV is highly diverse genetically and can be classified into 7 genotypes and multiple sub-types. Due to this antigenic variation, the induction of cross-reactive and at the same time neutralizing antibodies is a challenge in vaccine production. Here we report the analysis of immunogenicity of recombinant HCV envelope glycoproteins from genotypes 1a, 1b and 2a, with a Flag tag inserted in the hypervariable region 1 of E2. This modification did not affect protein expression or conformation or its capacity to bind the crucial virus entry factor, CD81. Importantly, in immunogenicity studies on mice, the purified E2-Flag mutants elicited high-titer, cross-reactive antibodies that were able to neutralize HCV infectious particles from two genotypes tested (1a and 2a). These findings indicate that E1E2-Flag envelope glycoproteins could be important immunogen candidates for vaccine aiming to induce broad HCV-neutralizing responses.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCell LineCross ReactionsEpitope MappingEpitopesGenotypeHepacivirusHumansImmunogenicity, VaccineMiceNeutralization TestsReceptors, VirusRecombinant ProteinsTetraspanin 28Antibodies, NeutralizingAntibodies, ViralE1 protein, Hepatitis C virusEpitopesglycoprotein E2, Hepatitis C virusReceptors, VirusRecombinant ProteinsTetraspanin 28Viral Envelope ProteinsE1E2Envelope glycoproteinsFlag tagHepatitis C virusNeutralizationVaccine

Identifiers

PMID29631174
PMCPMC5998380
OpenAlexW2795752972

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.