Evidence map›Paper›PMID 23405141›Full record

ArticlePloS one2013

TGF-β and TGF-β/Smad signaling in the interactions between Echinococcus multilocularis and its hosts.

Junhua Wang, Chuanshan Zhang, Xufa Wei, Oleg Blagosklonov, Guodong Lv, Xiaomei Lu, Georges Mantion, Dominique A Vuitton, Hao Wen, Renyong Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  6. Review
  7. Comprehensive analysis of gut microbiome and host transcriptome in chickens afterFrontiers in cellular and infection microbiology · 2023
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  8. Ghrelin regulating liver activity and its potential effects on liver fibrosis andFrontiers in cellular and infection microbiology · 2023
    Review
  9. Transforming growth factor-β signalling regulates protoscolex formation in theFrontiers in cellular and infection microbiology · 2023
    Article
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  13. Article
  14. Article
  15. Article
  16. miRNAs and lncRNAs inInternational journal of molecular sciences · 2020
    Review
  17. Kupffer Cells: Important Participant of Hepatic Alveolar Echinococcosis.Frontiers in cellular and infection microbiology · 2020
    Article
  18. Article
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  20. Article
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 3 institutions in 2 countries.

Junhua WangState Key Lab Incubation Base of Xinjiang Major Diseases Research (2010DS890294) and Xinjiang Key Laboratory of Echinococcosis, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Chuanshan Zhang
Xufa Wei
Oleg Blagosklonov
Guodong Lv
Xiaomei Lu
Georges Mantion
Dominique A Vuitton
Hao Wen
Renyong Lin
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNUniversité de franche-comté · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar echinococcosis (AE) is characterized by the development of irreversible fibrosis and of immune tolerance towards Echinococcus multilocularis (E. multilocularis). Very little is known on the presence of transforming growth factor-β (TGF-β) and other components of TGF-β/Smad pathway in the liver, and on their possible influence on fibrosis, over the various stages of infection. Using Western Blot, qRT-PCR and immunohistochemistry, we measured the levels of TGF-β1, TGF-β receptors, and down-stream Smads activation, as well as fibrosis marker expression in both a murine AE model from day 2 to 360 post-infection (p.i.) and in AE patients. TGF-β1, its receptors, and down-stream Smads were markedly expressed in the periparasitic infiltrate and also in the hepatocytes, close to and distant from AE lesions. Fibrosis was significant at 180 days p.i. in the periparasitic infiltrate and was also present in the liver parenchyma, even distant from the lesions. Over the time course after infection TGF-β1 expression was correlated with CD4/CD8 T-cell ratio long described as a hallmark of AE severity. The time course of the various actors of the TGF-β/Smad system in the in vivo mouse model as well as down-regulation of Smad7 in liver areas close to the lesions in human cases highly suggest that TGF-β plays an important role in AE both in immune tolerance against the parasite and in liver fibrosis.

Indexed as

ActinsAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCollagen Type ICollagen Type IIIDown-RegulationEchinococcosisEchinococcosis, HepaticEchinococcus multilocularisFemaleFibrosisHepatocytesHumansLiverMiceActinsalpha-smooth muscle actin, mouseCollagen Type ICollagen Type IIISmad7 ProteinSmad7 protein, mouseSmad ProteinsTransforming Growth Factor beta1

Identifiers

PMID23405141
PMCPMC3566151
OpenAlexW2003738054

What OpenQuestion holds

Textmetadata
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.