Evidence map›Paper›PMID 30767092›Full record

ArticleClinical rheumatology2019

Upregulated expression of STAT3/IL-17 in patients with systemic lupus erythematosus.

Shih-Yao Chen, Ming-Fei Liu, Pin-Yu Kuo, Chrong-Reen Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Systemic lupus erythematosus with high disease activity identification based on machine learning.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. The protective capability ofFrontiers in immunology · 2022
    Article
  10. Autoinducer-2 promotesFrontiers in microbiology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Cutaneous and systemic connections in lupus.Current opinion in rheumatology · 2020
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Shih-Yao ChenSection of Rheumatology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.
Ming-Fei LiuSection of Rheumatology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan.
Pin-Yu KuoDepartment of Microbiology and Immunology, National Cheng Kung University Medical College, Tainan, Taiwan.
Chrong-Reen WangSection of Rheumatology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan, Taiwan. wangcr@mail.ncku.edu.tw.
National Cheng Kung University · TWNational Cheng Kung University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated IL-17 levels with higher Th17 numbers are identified in systemic lupus erythematosus (SLE). STAT3 signaling plays a crucial role in the Th17 generation, and SOCS3 negatively regulates their formation. We investigated IL-17, STAT3, and SOCS3 expression, and analyzed their correlations to elucidate the regulatory mechanisms of IL-17 production in SLE. This study enrolled 32 patients, and venous mononuclear cells (MNCs) were isolated with further purification of CD4-positive T cells. IL-17 and SOCS3 levels were measured by real-time quantitative PCR, and pSTAT3/STAT3 expression was analyzed by immunoblot. Elevated IL-17 and SOCS3 levels were identified in lupus patients. There were higher IL-17 levels in lupus nephritis (class IV) than in SLE without renal involvement. Positive correlations were found between IL-17 levels and SOCS3 expression, lupus activity (SLEDAI-2K), or daily proteinuria. There were higher intensities of pSTAT3/β-actin and STAT3/β-actin in SLE, and a positive correlation between IL-17 expression and pSTAT3/β-actin or STAT3/β-actin intensity. Lupus nephritis (class IV) had higher STAT3/β-actin intensity than SLE without renal involvement. These results suggest upregulated STAT3/IL-17 expression in lupus patients. Such findings might facilitate the development of novel compounds and the application of existing therapeutics targeting the STAT3/IL-17 signal in SLE.

Indexed as

AdultCD4-Positive T-LymphocytesFemaleFlow CytometryHumansInterleukin-17Leukocytes, MononuclearLinear ModelsLupus Erythematosus, SystemicLupus NephritisMaleSignal TransductionSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinTaiwanTh17 CellsIL17A protein, humanInterleukin-17SOCS3 protein, humanSTAT3 protein, humanSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinIL-17Lupus nephritisSTAT3Systemic lupus erythematosus

Identifiers

PMID30767092
OpenAlexW2912942100

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.