Evidence map›Paper›PMID 23054344›Full record

ArticleJournal of clinical immunology2013

Expression of IL-27, Th1 and Th17 in patients with aplastic anemia.

Hui-zhen Du, Qian Wang, Jian Ji, Bao-ming Shen, Shao-chun Wei, Li-juan Liu, Juan Ding, Dao-xin Ma, Wen Wang, Jun Peng and 1 more

Abstract read
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In one paragraph

Article in Journal of clinical immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. IL-27-DependentInternational journal of molecular sciences · 2026
    Article
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  11. Review
  12. Modulation of inflammation by interleukin-27.Journal of leukocyte biology · 2013
    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

11 authors at 5 institutions in 1 country.

Hui-zhen DuLaiwu Central Hospital of Xinwen Mining Industry Group, Laiwu, Shandong, People's Republic of China.
Qian Wang
Jian Ji
Bao-ming Shen
Shao-chun Wei
Li-juan Liu
Juan Ding
Dao-xin Ma
Wen Wang
Jun Peng
Ming Hou
Qilu Hospital of Shandong University · CNHuainan Mining Industry Group (China) · CNShandong University · CNJinan City People's Hospital · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAplastic anemia (AA) is an autoimmune disease and interleukin-27 (IL-27) is an important cytokine involved in the pathogenesis of autoimmune diseases. To date there have been no reports concerning the intrinsic association among IL-27 and Thelper (Th) 1 and Th17 cells in AA. MATERIALS AND

methodsEnzyme-linked immunosorbent assay (ELISA) to assay IL-27, interferon gamma (IFN-γ) and IL-17 levels, flow cytometry to measure the percentages of Th1 and Th17 cells among peripheral blood mononuclear cells (PBMCs), real-time reverse transcriptase polymerase chain reaction (PCR) for the mRNA levels of IL-27, IFN-γ, T-bet and IL-17 and retinoid related orphan receptor gamma (RORγt) in PBMCs were performed. In addition, the effect of exogenous rhIL-27 on the differentiation of T cells into Th1 and Th17 cells was investigated in vitro.

resultsPlasma and mRNA levels of IL-27 in PBMCs from AA patients were significantly higher than those in healthy controls. A positive correlation was found between plasma levels of IL27 and IFN-γ. The proportions of Th1 and Th17 cells accompanied by the mRNA expression of RORγt and T-bet were significantly higher in AA patients than in healthy controls. Plasma levels of IL-27 correlated positively with frequencies of Th1 cells in AA patients. Exogenous rhIL-27 could significantly upregulate the frequency of Th1 cells and the mRNA levels of T-bet and IFN-γ and the application of rhIL-27 in vitro could inhibit the expression of RORγt mRNA.

conclusionThe upregulation of IL-27 might cause Th1 differentiation and immune disorders in AA patients. Blocking the expression of IL-27 could therefore be a reasonable therapeutic strategy for AA.

Indexed as

AdolescentAdultAgedAnemia, AplasticFemaleGene Expression RegulationHumansInterferon-gammaInterleukin-17MaleMiddle AgedNuclear Receptor Subfamily 1, Group F, Member 3RNA, MessengerT-bet Transcription FactorT-Box Domain ProteinsTh17 CellsInterferon-gammaInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3RNA, MessengerT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID23054344
OpenAlexW2034345991

What OpenQuestion holds

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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.