Evidence map›Paper›PMID 22896607›Full record

ArticleJournal of virology2012

Broadly neutralizing immune responses against hepatitis C virus induced by vectored measles viruses and a recombinant envelope protein booster.

Jorge Reyes-del Valle, Cynthia de la Fuente, Mallory A Turner, Christoph Springfeld, Swapna Apte-Sengupta, Marie E Frenzke, Amelie Forest, Jillian Whidby, Joseph Marcotrigiano, Charles M Rice and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. A safe and highly efficacious measles virus-based vaccine expressing SARS-CoV-2 stabilized prefusion spike.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Development of Recombinant Measles Virus-Based Vaccines.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Viral and Synthetic RNA Vector Technologies and Applications.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Review
  20. 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

11 authors at 3 institutions in 1 country.

Jorge Reyes-del ValleDepartment of Molecular Medicine and Virology and Gene Therapy Track, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Cynthia de la Fuente
Mallory A Turner
Christoph Springfeld
Swapna Apte-Sengupta
Marie E Frenzke
Amelie Forest
Jillian Whidby
Joseph Marcotrigiano
Charles M Rice
Roberto Cattaneo
Mayo Clinic · USRockefeller University · USRutgers, The State University of New Jersey · US

Funding

Translational CoreU19AI040034 · NIAID · STANFORD UNIVERSITY · PI RICE, CHARLES M · 1996 to 2009
$8.1M
Mechanistic Studies of HCV E2R01AI080659 · NIAID · RUTGERS, THE STATE UNIV OF N.J. · PI MARCOTRIGIANO, JOSEPH · 2010 to 2013
$1.5M
Measles Viruses with Added Vaccine SpecificitiesR01AI057761 · NIAID · MAYO CLINIC ROCHESTER · PI CATTANEO, ROBERTO B. · 2004 to 2007
$1.3M
NCRR NIH HHS RR11069NIAID NIH HHS AI 080659NIAID NIH HHS AI 57761NIAID NIH HHS R01 AI057761NIAID NIH HHS R01 AI080659NIAID NIH HHS U19 AI040034NIAID NIH HHS U19AI40034
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infection remains a serious public health problem worldwide. Treatments are limited, and no preventive vaccine is available. Toward developing an HCV vaccine, we engineered two recombinant measles viruses (MVs) expressing structural proteins from the prototypic HCV subtype 1a strain H77. One virus directs the synthesis of the HCV capsid (C) protein and envelope glycoproteins (E1 and E2), which fold properly and form a heterodimer. The other virus expresses the E1 and E2 glycoproteins separately, with each one fused to the cytoplasmic tail of the MV fusion protein. Although these hybrid glycoproteins were transported to the plasma membrane, they were not incorporated into MV particles. Immunization of MV-susceptible, genetically modified mice with either vector induced neutralizing antibodies to MV and HCV. A boost with soluble E2 protein enhanced titers of neutralizing antibody against the homologous HCV envelope. In animals primed with MV expressing properly folded HCV C-E1-E2, boosting also induced cross-neutralizating antibodies against two heterologous HCV strains. These results show that recombinant MVs retain the ability to induce MV-specific humoral immunity while also eliciting HCV neutralizing antibodies, and that anti-HCV immunity can be boosted with a single dose of purified E2 protein. The use of MV vectors could have advantages for pediatric HCV vaccination.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCross ReactionsDrug CarriersGenetic VectorsHepacivirusMeasles virusMiceVaccines, SubunitVaccines, SyntheticViral Envelope ProteinsViral VaccinesAntibodies, NeutralizingAntibodies, ViralDrug CarriersVaccines, SubunitVaccines, SyntheticViral Envelope ProteinsViral Vaccines

Identifiers

PMID22896607
PMCPMC3486281
OpenAlexW2136643186

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.