Evidence map›Paper›PMID 23161469›Full record

ArticleEuropean journal of immunology2013

HCV-infected hepatocytes drive CD4+ CD25+ Foxp3+ regulatory T-cell development through the Tim-3/Gal-9 pathway.

Xiao J Ji, Cheng J Ma, Jia M Wang, Xiao Y Wu, Toshiro Niki, Mitsumi Hirashima, Jonathan P Moorman, Zhi Q Yao

Open access · greenAbstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 77 citations in OpenAlex.

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  18. The role of Tim-3/Galectin-9 pathway in T-cell function and prognosis of patients with human papilloma virus-associated cervical carcinoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 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

8 authors at 6 institutions in 3 countries.

Xiao J JiDepartment of Internal Medicine, Division of Infectious Diseases, James H Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.
Cheng J Ma
Jia M Wang
Xiao Y Wu
Toshiro Niki
Mitsumi Hirashima
Jonathan P Moorman
Zhi Q Yao
East Tennessee State University · USCapital Medical University · CNGalena Biopharma (United States) · USKagawa University · JPSoochow University · CNUnited States Department of Veterans Affairs · US

Funding

Tim-3-mediated IL-12 dysregulation in antiviral responses to HCV infectionR01DK093526 · NIDDK · EAST TENNESSEE STATE UNIVERSITY · PI YAO, ZHI Q. · 2012 to 2015
$1.2M
The role of PD-1 and SOCS-1 in HCV core/gC1qR-mediated IL-12 suppressionR15AI084057 · NIAID · EAST TENNESSEE STATE UNIVERSITY · PI YAO, ZHI Q. · 2009 to 2009
$215k
NIAID NIH HHS R15 AI084057NIDDK NIH HHS R01 DK093526NIDDK NIH HHS R01DK093526PHS HHS 1R15A1084057
6 · The paper itself

Abstract

HCV is remarkable at disrupting human immunity to establish chronic infection. The accumulation of Treg cells at the site of infection and upregulation of inhibitory signaling pathways (such as T-cell Ig and mucin domain protein-3 (Tim-3) and galectin-9 (Gal-9)) play pivotal roles in suppressing antiviral effector T (Teff) cells that are essential for viral clearance. While Tim-3/Gal-9 interactions have been shown to negatively regulate Teff cells, their role in regulating Treg cells is poorly understood. To explore how Tim-3/Gal-9 interactions regulate HCV-mediated Treg-cell development, here we provide pilot data showing that HCV-infected human hepatocytes express higher levels of Gal-9 and TGF-β, and upregulate Tim-3 expression and regulatory cytokines TGF-β/IL-10 in co-cultured human CD4(+) T cells, driving conventional CD4(+) T cells into CD25(+) Foxp3(+) Treg cells. Additionally, recombinant Gal-9 protein can transform TCR-activated CD4(+) T cells into Foxp3(+) Treg cells in a dose-dependent manner. Importantly, blocking Tim-3/Gal-9 ligations abrogates HCV-mediated Treg-cell induction by HCV-infected hepatocytes, suggesting that Tim-3/Gal-9 interactions may regulate human Foxp3(+) Treg-cell development and function during HCV infection.

Indexed as

CD4-Positive T-LymphocytesCells, CulturedCoculture TechniquesForkhead Transcription FactorsGalectinsHepacivirusHepatitis A Virus Cellular Receptor 2Hepatitis C, ChronicHepatocytesHumansInterleukin-2 Receptor alpha SubunitMembrane ProteinsT-Lymphocytes, RegulatoryTransforming Growth Factor betaForkhead Transcription FactorsFOXP3 protein, humanGalectinsHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2IL2RA protein, humanInterleukin-2 Receptor alpha SubunitLGALS9 protein, humanMembrane ProteinsTransforming Growth Factor beta

Identifiers

PMID23161469
PMCPMC3757554
OpenAlexW2113649995

What OpenQuestion holds

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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.