Evidence map›Paper›PMID 23551262›Full record

ArticleImmunology2013

Characteristics of IL-17 induction by Schistosoma japonicum infection in C57BL/6 mouse liver.

Dianhui Chen, Xueping Luo, Hongyan Xie, Zhiyan Gao, Huilong Fang, Jun Huang

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The IL-17 family in diseases: from bench to bedside.Signal transduction and targeted therapy · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Whole blood transcriptome analysis in onchocerciasis.Current research in parasitology & vector-borne diseases · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Molecular Mechanisms ofFrontiers in cell and developmental biology · 2021
    Review
  16. Article
  17. Sja-miR-71a inJournal of extracellular vesicles · 2020
    Article
  18. Article
  19. Review
  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

6 authors at 2 institutions in 1 country.

Dianhui ChenDepartment of Pathogenic Biology and Immunology, Guangzhou Medical College, Guangzhou, China.
Xueping Luo
Hongyan Xie
Zhiyan Gao
Huilong Fang
Jun Huang
Guangzhou Medical University · CNXiangnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schistosomiasis japonica is a severe tropical disease caused by the parasitic worm Schistosoma japonicum. Among the most serious pathological effects of S. japonicum infection are hepatic lesions (cirrhosis and fibrosis) and portal hypertension. Interleukin-17 (IL-17) is a pro-inflammatory cytokine involved in the pathogenesis of many inflammatory and infectious conditions, including schistosomiasis. We infected C57BL/6 mice with S. japonicum and isolated lymphocytes from the liver to identify cell subsets with high IL-17 expression and release using flow cytometry and ELISA. Expression and release of IL-17 was significantly higher in hepatic lymphocytes from infected mice compared with control mice in response to both non-specific stimulation with anti-CD3 monoclonal antibody plus/anti-CD28 monoclonal antibody and PMA plus ionomycin. We then compared IL-17 expression in three hepatic T-cell subsets, T helper, natural killer T and γδT cells, to determine the major source of IL-17 during infection. Interleukin-17 was induced in all three subsets by PMA + ionomycin, but γδT lymphocytes exhibited the largest increase in expression. We then established a mouse model to further investigate the role of IL-17 in granulomatous and fibrosing inflammation against parasite eggs. Reducing IL-17 activity using anti-IL-17A antibodies decreased infiltration of inflammatory cells and collagen deposition in the livers of infected C57BL/6 mice. The serum levels of soluble egg antigen (IL)-specific IgGs were enhanced by anti-IL-17A monoclonal antibody blockade, suggesting that IL-17 normally serves to suppress this humoral response. These findings suggest that γδT cells are the most IL-17-producing cells and that IL-17 contributes to granulomatous inflammatory and fibrosing reactions in S. japonicum-infected C57BL/6 mouse liver.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ProtozoanCells, CulturedCollagen Type IIIDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryGranulomaInflammation MediatorsInterleukin-17IonomycinLiverLiver CirrhosisAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ProtozoanCollagen Type IIIIl17a protein, mouseInflammation MediatorsInterleukin-17IonomycinReceptors, Antigen, T-Cell, gamma-deltainterleukin-17livernatural killer T cellSchistosoma japonicumT helper type 17γδT cell

Identifiers

PMID23551262
PMCPMC3719069
OpenAlexW2079570367

What OpenQuestion holds

Textmetadata
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.