Evidence map›Paper›PMID 26728971›Full record

ArticleScientific reports2016

A deleterious role for Th9/IL-9 in hepatic fibrogenesis.

Shan-yu Qin, Dong-hong Lu, Xiao-yun Guo, Wei Luo, Bang-li Hu, Xiao-li Huang, Mei Chen, Jia-xu Wang, Shi-Jia Ma, Xian-wen Yang and 2 more

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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

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  14. Interleukin-9 in Immunopathology ofFrontiers in cellular and infection microbiology · 2021
    Article
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  18. Review
  19. Article
  20. Dusting Off IL-9 as a New Therapeutic Target for Pulmonary Fibrosis.American journal of respiratory cell and molecular biology · 2019
    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

12 authors at 3 institutions in 3 countries.

Shan-yu QinDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Dong-hong LuDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Xiao-yun GuoDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Wei LuoDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Bang-li HuDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Xiao-li HuangDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Mei ChenDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Jia-xu WangDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Shi-Jia MaDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Xian-wen YangDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Hai-xing JiangDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
You ZhouSystems Immunity University Research Institute, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Guangxi Medical University · CNFirst Affiliated Hospital of GuangXi Medical University · CNCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T helper 9 (Th9) cells, a recently recognized Th cell subset, are involved in autoimmune diseases. We aimed to investigate the role of Th9/interleukin-9 (IL-9) in the pathogenesis of hepatic fibrosis. Th9 and Th17 cells were quantified in chronic hepatitis B (CHB) patients with hepatic fibrosis, HBV-associated liver cirrhosis (LC) patients and healthy controls (HC). The percentages of Th9 and Th17 cells, concentrations of IL-9 and IL-17, as well as expression of IL-17, TNF-α, IL-6, IL-4, IL-21, TGF-β1 and IFN-γ were significantly increased in plasma of CHB and LC patients compared with those in HC. Splenic Th9 and Th17 cells, plasma concentrations and liver expression of IL-9 and IL-17A were significantly elevated in mice with hepatic fibrosis compared with controls. Neutralization of IL-9 in mice ameliorated hepatic fibrosis, attenuated the activation of hepatic stellate cells, reduced frequencies of Th9, Th17 and Th1 cells in spleen, and suppressed expression of IL-9, IL-17A, IFN-γ, TGF-β1, IL-6, IL-4 and TNF-α in plasma and liver respectively. Our data suggest a deleterious role of Th9/IL-9 in increasing hepatic fibrosis and exacerbating disease endpoints, indicating that Th9/IL9 based immunotherapy may be a promising approach for treating hepatic fibrosis.

Indexed as

T-Lymphocyte SubsetsAdolescentAdultAgedAnimalsAntibodies, MonoclonalAntibodies, NeutralizingCase-Control StudiesCytokinesDisease Models, AnimalFemaleHepatitis B, ChronicHumansImmunophenotypingInterleukin-17Interleukin-9Antibodies, MonoclonalAntibodies, NeutralizingCytokinesInterleukin-17Interleukin-9RNA, Messenger

Identifiers

PMID26728971
PMCPMC4700496
OpenAlexW2223918717

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.