Evidence map›Paper›PMID 20529250›Full record

ArticleVirology journal2010

Intracytoplasmic stable expression of IgG1 antibody targeting NS3 helicase inhibits replication of highly efficient hepatitis C Virus 2a clone.

Partha K Chandra, Sidhartha Hazari, Bret Poat, Feyza Gunduz, Ramesh Prabhu, Gerald Liu, Roberto Burioni, Massimo Clementi, Robert F Garry, Srikanta Dash

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Virology journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-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

10 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Partha K ChandraDepartment of Pathology and Laboratory Medicine, Tulane University Health Sciences Center, 1430 Tulane Avenue, New Orleans, LA-70112, USA.
Sidhartha Hazari
Bret Poat
Feyza Gunduz
Ramesh Prabhu
Gerald Liu
Roberto Burioni
Massimo Clementi
Robert F Garry
Srikanta Dash
Tulane University · USVita-Salute San Raffaele University · IT

Funding

Peptide inhbitors of influenza entry-FAST TRACKR44AI082778 · NIAID · AUTOIMMUNE TECHNOLOGIES, LLC · PI WILSON, RUSSELL B · 2009 to 2011
$3.9M
Hepatocarcinogenesis Secondary to Hepatitis CR01CA127481 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI DASH, SRIKANTA · 2008 to 2012
$1.4M
HIV-1 Tat modulation of HCV replication and pathogenesisR21DK070551 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI GARRY, ROBERT F · 2005 to 2006
$440k
Intracellular immunization strategy in inhibit HCV related liver cancerR21CA129776 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI DASH, SRIKANTA · 2009 to 2010
$343k
Peptide inhibitors of dengue virus infectivityR56AI064617 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI GARRY, ROBERT F · 2006 to 2006
$304k
NCI NIH HHS CA127481NCI NIH HHS CA129776NIAID NIH HHS R44AI082778NIAID NIH HHS R56AI64617NIDDK NIH HHS R21DK070551
6 · The paper itself

Abstract

backgroundHepatitis C virus (HCV) infection is a major public health problem with more than 170 million cases of chronic infections worldwide. There is no protective vaccine currently available for HCV, therefore the development of novel strategy to prevent chronic infection is important. We reported earlier that a recombinant human antibody clone blocks viral NS3 helicase activity and inhibits replication of HCV 1b virus. This study was performed further to explore the mechanism of action of this recombinant antibody and to determine whether or not this antibody inhibits replication and infectivity of a highly efficient JFH1 HCV 2a virus clone.

resultsThe antiviral effect of intracellular expressed antibody against the HCV 2a virus strain was examined using a full-length green fluorescence protein (GFP) labeled infectious cell culture system. For this purpose, a Huh-7.5 cell line stably expressing the NS3 helicase gene specific IgG1 antibody was prepared. Replication of full-length HCV-GFP chimera RNA and negative-strand RNA was strongly inhibited in Huh-7.5 cells stably expressing NS3 antibody but not in the cells expressing an unrelated control antibody. Huh-7.5 cells stably expressing NS3 helicase antibody effectively suppressed infectious virus production after natural infection and the level of HCV in the cell free supernatant remained undetectable after first passage. In contrast, Huh-7.5 cells stably expressing an control antibody against influenza virus had no effect on virus production and high-levels of infectious HCV were detected in culture supernatants over four rounds of infectivity assay. A recombinant adenovirus based expression system was used to demonstrate that Huh-7.5 replicon cell line expressing the intracellular antibody strongly inhibited the replication of HCV-GFP RNA.

conclusionRecombinant human anti-HCV NS3 antibody clone inhibits replication of HCV 2a virus and infectious virus production. Intracellular expression of this recombinant antibody offers a potential antiviral strategy to inhibit intracellular HCV replication and production.

Indexed as

Gene ExpressionVirus ReplicationCell LineCytoplasmDEAD-box RNA HelicasesDown-RegulationHepacivirusHepatitis CHumansImmunoglobulin GNucleoside-TriphosphataseSerine EndopeptidasesViral Nonstructural ProteinsViral ProteasesDEAD-box RNA HelicasesImmunoglobulin GNS3 protein, hepatitis C virusNucleoside-TriphosphataseSerine EndopeptidasesViral Nonstructural ProteinsViral Proteases

Identifiers

PMID20529250
PMCPMC2903558
OpenAlexW2006311979

What OpenQuestion holds

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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.