Evidence map›Paper›PMID 26879672›Full record

ArticleScientific reports2016

(-)-Epigallocatechin-3-Gallate Enhances Hepatitis C Virus Double-Stranded RNA Intermediates-Triggered Innate Immune Responses in Hepatocytes.

Yizhong Wang, Jieliang Li, Xu Wang, Juliet C Peña, Kui Li, Ting Zhang, Wenzhe Ho

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

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  12. Epigallocatechin-3-gallate Can Prevent Type 2 Human PapillomavirusInternational journal of molecular sciences · 2021
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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

7 authors at 4 institutions in 2 countries.

Yizhong WangDepartment of Infectious Diseases, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai 200040, P.R. China.
Jieliang LiDepartment of Pathology and Laboratory Medicine, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Xu WangDepartment of Pathology and Laboratory Medicine, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Juliet C PeñaDepartment of Pathology and Laboratory Medicine, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Kui LiDeparment of Microbiology, Immunology, and Biochemistry, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Ting ZhangDepartment of Infectious Diseases, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai 200040, P.R. China.
Wenzhe HoDepartment of Pathology and Laboratory Medicine, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Temple University · USShanghai Children's Hospital · CNShanghai Jiao Tong University · CNUniversity of Tennessee Health Science Center · US

Funding

Opioids, HIV/HCV and Host Cell Innate ImmunityR01DA022177 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2007 to 2017
$2.9M
Role of TLR3 Signaling in Control of HCVR01AI069285 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI LI, KUI · 2007 to 2016
$2.5M
Opioids, LPS and HIVR01DA027550 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2010 to 2014
$1.4M
Opioid, Astroglial TLR3/RIG-I Signaling and HIVR21DA036163 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2013 to 2014
$426k
Role of TLR3 Signaling in Control of HCVR56AI069285 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LI, KUI · 2012 to 2012
$300k
Methamphetamine, Brain Endothelial TLR3 Signaling and HIVR03DA036413 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI LI, JIELIANG · 2014 to 2015
$155k
NIAID NIH HHS AI069285NIAID NIH HHS R01 AI069285NIAID NIH HHS R56 AI069285NIDA NIH HHS DA022177NIDA NIH HHS DA027550NIDA NIH HHS DA036163NIDA NIH HHS DA036413NIDA NIH HHS R01 DA022177NIDA NIH HHS R01 DA027550NIDA NIH HHS R03 DA036413NIDA NIH HHS R21 DA036163
6 · The paper itself

Abstract

(-)-Epigallocatechin-3-gallate (EGCG), a major polyphenol component of green tea, has recently been identified as an inhibitor of hepatitis C virus (HCV) entry. Here, we examined whether EGCG can enhance hepatocyte-mediated intracellular innate immunity against HCV. HCV dsRNAs (Core, E1-P7, NS-3'NTR and NS5A) induced interferon-λ1 (IFN-λ1) expression in human hepatocytes. These HCV dsRNAs also induced the expression of Toll-like receptor 3 (TLR3), retinoic acid-inducible gene I (RIG-I) and several antiviral IFN-stimulated genes (ISGs) expression. Although EGCG treatment of hepatocytes alone had little effect on TLR3 and RIG-I signaling pathways, EGCG significantly enhanced HCV dsRNAs-induced the expression of IFN-λ1, TLR3, RIG-I and antiviral ISGs in hepatocytes. Furthermore, treatment of HCV-infected hepatocytes with EGCG and HCV dsRNAs inhibited viral replication. Given that EGCG has the ability to enhance HCV dsRNAs-induced intracellular antiviral innate immunity against HCV, suggesting the potential application of EGCG as a new anti-HCV agent for HCV therapy.

Indexed as

Antiviral AgentsCatechinCell Line, TumorDEAD Box Protein 58HepacivirusHepatocytesHumansImmunity, InnateInterferon LambdaInterferonsInterleukinsReceptors, ImmunologicRNA, Double-StrandedRNA, ViralSignal TransductionToll-Like Receptor 3Antiviral AgentsCatechinDEAD Box Protein 58epigallocatechin gallateInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsReceptors, ImmunologicRIGI protein, humanRNA, Double-StrandedRNA, ViralTLR3 protein, humanToll-Like Receptor 3

Identifiers

PMID26879672
PMCPMC4754899
OpenAlexW2275598514

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.