Evidence map›Paper›PMID 21068233›Full record

ArticleJournal of virology2011

Spatial configuration of hepatitis E virus antigenic domain.

Li Xing, Joseph C Wang, Tian-Cheng Li, Yasuhiro Yasutomi, James Lara, Yury Khudyakov, Darren Schofield, Suzanne U Emerson, Robert H Purcell, Naokazu Takeda and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Hepatitis E virus: from innate sensing to adaptive immune responses.Nature reviews. Gastroenterology & hepatology · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Genetic Evolution of Hepatitis E Virus.Advances in experimental medicine and biology · 2023
    Review
  18. Prophylactic Hepatitis E Vaccine.Advances in experimental medicine and biology · 2023
    Article
  19. Article
  20. 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

12 authors at 6 institutions in 3 countries.

Li XingMolecular and Cellular Biology, University of California, 1 Shields Ave., Davis, CA 95616, USA.
Joseph C Wang
Tian-Cheng Li
Yasuhiro Yasutomi
James Lara
Yury Khudyakov
Darren Schofield
Suzanne U Emerson
Robert H Purcell
Naokazu Takeda
Tatsuo Miyamura
R Holland Cheng
National Institute of Allergy and Infectious Diseases · USNational Institute of Infectious Diseases · JPCenters for Disease Control and Prevention · USUniversity of California, Davis · USKarolinska Institutet · SENational Institute of Biomedical Innovation, Health and Nutrition · JP

Funding

In Vivo And In Vitro Studies Of Hepatitis E VirusZIAAI000596 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI EMERSON, SUZANNE U · 2009 to 2014
$3.4M
New Approaches To Active ImmunoprophylaxisZIAAI000823 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PURCELL, ROBERT H. · 2009 to 2012
$2.6M
Present Homologous and Heterologous Antigen with Hepatitis E VirusR56AI095382 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHENG, R.HOLLAND · 2012 to 2012
$385k
NIAID NIH HHS R56 AI095382
6 · The paper itself

Abstract

Hepatitis E virus (HEV) is a human pathogen that causes acute hepatitis. When an HEV capsid protein containing a 52-amino-acid deletion at the C terminus and a 111-amino-acid deletion at the N terminus is expressed in insect cells, the recombinant HEV capsid protein can self-assemble into a T=1 virus-like particle (VLP) that retains the antigenicity of the native HEV virion. In this study, we used cryoelectron microscopy and image reconstruction to show that anti-HEV monoclonal antibodies bind to the protruding domain of the capsid protein at the lateral side of the spikes. Molecular docking of the HEV VLP crystal structure revealed that Fab224 covered three surface loops of the recombinant truncated second open reading frame (ORF2) protein (PORF2) at the top part of the spike. We also determined the structure of a chimeric HEV VLP and located the inserted B-cell tag, an epitope of 11 amino acids coupled to the C-terminal end of the recombinant ORF2 protein. The binding site of Fab224 appeared to be distinct from the location of the inserted B-cell tag, suggesting that the chimeric VLP could elicit immunity against both HEV and an inserted foreign epitope. Therefore, the T=1 HEV VLP is a novel delivery system for displaying foreign epitopes at the VLP surface in order to induce antibodies against both HEV and the inserted epitope.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, ViralAntigens, ViralCapsid ProteinsCell LineCryoelectron MicroscopyEpitopesFemaleHepatitis E virusImage Processing, Computer-AssistedMiceMice, Inbred BALB CModels, MolecularProtein BindingProtein MultimerizationAntibodies, MonoclonalAntibodies, ViralAntigens, ViralCapsid ProteinsEpitopesVirosomes

Identifiers

PMID21068233
PMCPMC3020005
OpenAlexW2130134384

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.