Evidence map›Paper›PMID 17050612›Full record

ArticleJournal of virology2007

Initiation of hepatitis C virus infection is dependent on cholesterol and cooperativity between CD81 and scavenger receptor B type I.

Sharookh B Kapadia, Heidi Barth, Thomas Baumert, Jane A McKeating, Francis V Chisari

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 143 papers.

0numbers the graph read from it
0cells of the map it votes in
143citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

143 citing papers in PubMed, 256 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Identification of claudin-3 as an entry factor for rat hepacivirus.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Review
  15. Atorvastatin Rapidly Reduces Hepatitis B Viral Load in Combination with Tenofovir: A Prospective Clinical Trial.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2022
    Article
  16. Entry Inhibitors of Hepatitis C Virus.Advances in experimental medicine and biology · 2022
    Article
  17. Review
  18. Thiol-Mediated Uptake.JACS Au · 2021
    Review
  19. Article
  20. Article

83 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Sharookh B KapadiaDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Heidi Barth
Thomas Baumert
Jane A McKeating
Francis V Chisari
Scripps Research Institute · USUniversity of Freiburg · DENIHR Birmingham Biomedical Research Centre · GB

Funding

CELLULAR GENES THAT CONTROL HCV REPLICATIONR01CA108304 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI CHISARI, FRANCIS VINCENT · 2003 to 2007
$1.9M
Functional analysis of hepatitis C virus glycoproteinsR01AI050798 · NIAID · UNIVERSITY OF BIRMINGHAM · PI MCKEATING, JANE A. · 2004 to 2008
$1.3M
Medical Research Council G0400802Medical Research Council G0801976NCI NIH HHS CA108304NCI NIH HHS R01 CA108304NIAID NIH HHS AI50798NIAID NIH HHS R01 AI050798
6 · The paper itself

Abstract

In the past several years, a number of cellular proteins have been identified as candidate entry receptors for hepatitis C virus (HCV) by using surrogate models of HCV infection. Among these, the tetraspanin CD81 and scavenger receptor B type I (SR-BI), both of which localize to specialized plasma membrane domains enriched in cholesterol, have been suggested to be key players in HCV entry. In the current study, we used a recently developed in vitro HCV infection system to demonstrate that both CD81 and SR-BI are required for authentic HCV infection in vitro, that they function cooperatively to initiate HCV infection, and that CD81-mediated HCV entry is, in part, dependent on membrane cholesterol.

Indexed as

Anticholesteremic AgentsAntigens, CDbeta-CyclodextrinsCell LineCholesterolGene Expression RegulationHepacivirusHumansRepliconRNA, ViralScavenger Receptors, Class BTetraspanin 28Anticholesteremic AgentsAntigens, CDbeta-CyclodextrinsCD81 protein, humanCholesterolmethyl-beta-cyclodextrinRNA, ViralScavenger Receptors, Class BTetraspanin 28

Identifiers

PMID17050612
PMCPMC1797271
OpenAlexW2157816482

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.