Evidence map›Paper›PMID 9835618›Full record

ArticleThe Journal of clinical investigation1998

Pivotal role of TARC, a CC chemokine, in bacteria-induced fulminant hepatic failure in mice.

H Yoneyama, A Harada, T Imai, M Baba, O Yoshie, Y Zhang, H Higashi, M Murai, H Asakura, K Matsushima

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
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  7. IL-17A Can PromoteFrontiers in immunology · 2019
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  9. Myeloid Cells and Chronic Liver Disease: a Comprehensive Review.Clinical reviews in allergy & immunology · 2018
    Review
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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

10 authors at 4 institutions in 1 country.

H YoneyamaDepartment of Molecular Preventive Medicine, School of Medicine, and CREST, The University of Tokyo, Tokyo 113, Japan.
A Harada
T Imai
M Baba
O Yoshie
Y Zhang
H Higashi
M Murai
H Asakura
K Matsushima
The University of Tokyo · JPNiigata University · JPShionogi (Japan) · JPKindai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymus and activation-regulated chemokine (TARC) is a recently identified lymphocyte-directed CC chemokine which specifically chemoattracts T helper type 2 CD4(+) T cells in human. To establish the pathophysiological roles of TARC in vivo, we investigated whether a monoclonal antibody (mAb) against TARC could inhibit the induction of hepatic lesions in murine model using Propionibacterium acnes and lipopolysaccharide (LPS). P. acnes-induced intrahepatic granuloma formation in the priming phase is essential to the subsequent liver injury elicited by a low dose of LPS. The priming phase appears to be dominated by Th1 type immune responses determined by the profile of chemokine and chemokine receptor expression. TARC was selectively produced by granuloma-forming cells, and CC chemokine receptor 4 (CCR4)-expressing CD4(+) T cells migrated into the liver after LPS administration. In vivo injection of anti-TARC mAb just before LPS administration protected the mice from acute lethal liver damage, which was accompanied by a significant reduction of both CCR4 mRNA expression and IL-4 production by liver-infiltrating CD4(+) T cells. Moreover, both TNF-alpha and Fas ligand expressions in the liver were decreased by anti-TARC treatment. These results suggest that recruitment of IL-4-producing CCR4(+) CD4(+) T cells by granuloma-derived TARC into the liver parenchyma may be a key cause of massive liver injury after systemic LPS administration.

Indexed as

Propionibacterium acnesAnimalsAntibodies, MonoclonalBiomarkersChemokine CCL17Chemokines, CCFemaleGram-Positive Bacterial InfectionsGranulomaHepatic EncephalopathyLipopolysaccharidesMiceMice, Inbred BALB CReceptors, CCR4Receptors, ChemokineSpecific Pathogen-Free OrganismsAntibodies, MonoclonalBiomarkersCcl17 protein, mouseCCR4 protein, humanCcr4 protein, mouseChemokine CCL17Chemokines, CCLipopolysaccharidesReceptors, CCR4Receptors, ChemokineTranscription Factors

Identifiers

PMID9835618
PMCPMC509145
OpenAlexW2020554497

What OpenQuestion holds

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Registered trials

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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.