Evidence map›Paper›PMID 19821484›Full record

ArticleHepatology (Baltimore, Md.)2009

Mechanistic insights into immunomodulation by hepatic stellate cells in mice: a critical role of interferon-gamma signaling.

Horng-Ren Yang, Hong-Shuie Chou, Xiaodong Gu, Lianfu Wang, Kathleen E Brown, John J Fung, Lina Lu, Shiguang Qian

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.4field-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

45 citing papers in PubMed, 71 citations in OpenAlex.

  1. Clinicopathological features of graft versus host disease-associated myositis.Annals of clinical and translational neurology · 2024
    Review
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  14. Novel Effector Phenotype of Tim-3Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  15. Article
  16. Article
  17. Presentation of hepatocellular antigens.Cellular & molecular immunology · 2016
    Review
  18. Immunological aspects of liver cell transplantation.World journal of transplantation · 2016
    Review
  19. Hepatic Stellate Cells Directly Inhibit B Cells via Programmed Death-Ligand 1.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  20. Mechanisms of adaptation and progression in idiosyncratic drug induced liver injury, clinical implications.Liver international : official journal of the International Association for the Study of the Liver · 2016
    Review
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 2 institutions in 1 country.

Horng-Ren YangDepartment of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.
Hong-Shuie Chou
Xiaodong Gu
Lianfu Wang
Kathleen E Brown
John J Fung
Lina Lu
Shiguang Qian
Cleveland Clinic · USCleveland Clinic Lerner College of Medicine · US

Funding

Towards Induction of Cell Transplant ToleranceR01DK084192 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI LU, LINA · 2010 to 2014
$1.7M
Liver-Induced Activated T Cell DeathR01DK058316 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI QIAN, SHIGUANG · 2002 to 2004
$844k
NIDDK NIH HHS DK58316NIDDK NIH HHS R01 DK058316NIDDK NIH HHS R01 DK084192
6 · The paper itself

Abstract

unlabelledThe liver is considered to be an immune-privileged organ that favors the induction of tolerance. The underlying mechanisms are not completely understood. Interestingly, liver transplants are spontaneously accepted in several animal models, but hepatocyte transplants are acutely rejected, suggesting that liver nonparenchymal cells may effectively protect the parenchymal cells from immune attack. We have shown the profound T cell inhibitory activity of hepatic stellate cells (HSCs). Thus, cotransplantation with HSCs effectively protects islet allografts from rejection in mice. In this study, using T cell receptor transgenic and gene knockout approaches, we provided definitive evidence that HSCs protected cotransplanted islet allografts by exerting comprehensive inhibitory effects on T cells, including apoptotic death in graft-infiltrating antigen-specific effector T cells and marked expansion of CD4(+) Forkhead box protein (Foxp)3(+) T regulatory (Treg) cells. All these effects required an intact interferon-gamma (IFN-gamma) signaling in HSCs, demonstrated by using HSCs isolated from IFN-gamma receptor 1 knockout mice. B7-H1 expression on HSCs, a product molecule of IFN-gamma signaling, was responsible for induction of T cells apoptosis, but had no effect on expansion of Treg cells, suggesting that undetermined effector molecules produced by IFN-gamma signaling is involved in this process.

conclusionUpon inflammatory stimulation, specific organ stromal cells (such as HSCs in the liver) demonstrate potent immune regulatory activity. Understanding of the mechanisms involved may lead to development of novel strategies for clinical applications in transplantation and autoimmune diseases.

Indexed as

AnimalsApoptosisB7-1 AntigenB7-H1 AntigenCD8-Positive T-LymphocytesForkhead Transcription FactorsHepatic Stellate CellsInterferon-gammaInterferon gamma ReceptorIslets of Langerhans TransplantationMaleMembrane GlycoproteinsMiceMice, Inbred StrainsPeptidesReceptors, InterferonB7-1 AntigenB7-H1 AntigenCd274 protein, mouseForkhead Transcription FactorsFoxp3 protein, mouseInterferon-gammaInterferon gamma ReceptorMembrane GlycoproteinsPeptidesReceptors, Interferon

Identifiers

PMID19821484
PMCPMC2896244
OpenAlexW1985569603

What OpenQuestion holds

Textmetadata
LicenceTDM
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.