Evidence map›Paper›PMID 20600021›Full record

ArticleGastroenterology2010

Production of infectious hepatitis C virus in primary cultures of human adult hepatocytes.

Philippe Podevin, Arnaud Carpentier, Véronique Pène, Lynda Aoudjehane, Matthieu Carrière, Sakina Zaïdi, Céline Hernandez, Vanessa Calle, Jean-François Méritet, Olivier Scatton and 8 more

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Article in Gastroenterology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 150 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 8 institutions in 3 countries.

Philippe PodevinINSERM, Equipe Avenir Virologie de l'Hépatite C, Institut Cochin, Paris, France.
Arnaud Carpentier
Véronique Pène
Lynda Aoudjehane
Matthieu Carrière
Sakina Zaïdi
Céline Hernandez
Vanessa Calle
Jean-François Méritet
Olivier Scatton
Marlène Dreux
François-Loïc Cosset
Takaji Wakita
Ralf Bartenschlager
Sylvie Demignot
Filoména Conti
Arielle R Rosenberg
Yvon Calmus
Délégation Paris 5 · FRInserm · FRInstitut Cochin · FRAssistance Publique – Hôpitaux de Paris · FRCentre de Recherche des Cordeliers · FRGroupe Hospitalier Cochin - Port-Royal, Hôtel-Dieu, Broca - La Collégiale · FRHeidelberg University · DENational Institute of Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsAlthough hepatitis C virus (HCV) can be grown in the hepatocarcinoma-derived cell line Huh-7, a cell-culture model is needed that supports its complete, productive infection cycle in normal, quiescent, highly differentiated human hepatocytes. We sought to develop such a system.

methodsPrimary cultures of human adult hepatocytes were inoculated with HCV derived from Huh-7 cell culture (HCVcc) and monitored for expression of hepatocyte differentiation markers and replication of HCV. Culture supernatants were assayed for HCV RNA, core antigen, and infectivity titer. The buoyant densities of input and progeny virus were compared in iodixanol gradients.

resultsWhile retaining expression of differentiation markers, primary hepatocytes supported the complete infectious cycle of HCV, including production of significant titers of new infectious progeny virus, which was called primary-culture-derived virus (HCVpc). Compared with HCVcc, HCVpc had lower average buoyant density and higher specific infectivity; this was similar to the characteristics of virus particles associated with the very-low-density lipoproteins that are produced during in vivo infection. These properties were lost after re-culture of HCVpc in poorly differentiated Huh-7 cells, suggesting that authentic virions can be produced only by normal hepatocytes that secrete authentic very-low-density lipoproteins.

conclusionsWe have established a cell-culture-based system that allows production of infectious HCV in physiologically relevant human hepatocytes. This provides a useful tool for the study of HCV interactions with its natural host cell and for the development of antiviral therapies.

Indexed as

Virus ReplicationAdultCell DifferentiationCell Line, TumorGenome, ViralHepacivirusHepatocytesHumans

Identifiers

PMID20600021
OpenAlexW2036761416

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.