Evidence map›Paper›PMID 21487830›Full record

ArticleClinical and experimental medicine2011

Expressions of IL-22 in circulating CD4+/CD8+ T cells and their correlation with disease activity in SLE patients.

Wei-Zi Qin, Li-Li Chen, Hai-Feng Pan, Rui-Xue Leng, Zhi-Min Zhai, Chao Wang, Ruo-Jie Li, Song Wang, Hui-Ping Wang, Dong-Qing Ye

Abstract read
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Article in Clinical and experimental medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

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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

16 citing papers in PubMed, 37 citations in OpenAlex.

  1. Combined assessment of 25(OH)D, CD4Frontiers in immunology · 2026
    Article
  2. Review
  3. IL-22, a vital cytokine in autoimmune diseases.Clinical and experimental immunology · 2024
    Review
  4. Article
  5. T Cells in Systemic Lupus Erythematosus.Rheumatic diseases clinics of North America · 2021
    Review
  6. Elevated levels of CCR6Scientific reports · 2017
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Emerging role of interleukin-22 in autoimmune diseases.Cytokine & growth factor reviews · 2013
    Review
  14. Article
  15. Article
  16. 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 2 institutions in 1 country.

Wei-Zi QinDepartment of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, People's Republic of China.
Li-Li Chen
Hai-Feng Pan
Rui-Xue Leng
Zhi-Min Zhai
Chao Wang
Ruo-Jie Li
Song Wang
Hui-Ping Wang
Dong-Qing Ye
Anhui Medical University · CNSecond Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, Th17 cell-associated responses have received growing attention; however, the role of IL-22 (a cytokines also produced by Th17 cells) in the pathogenesis of systemic lupus erythematosus (SLE) has not been widely explored. In this study, we analyze the frequencies of IL-22-positive CD4+/CD8+ T cells in peripheral blood mononuclear cells (PBMCs) from patients with SLE and their correlations with disease activity and clinical data. Five-color flow cytometry (FCM) was used to assess IL-22 production of CD4+/CD8+ T cells in PBMCs from 31 patients with SLE and 22 healthy control subjects, following stimulation ex vivo with phorbol 12-myristate 13-acetate and ionomycin for 4 h. Results showed that the percentages of IL-22-positive CD4+ T cells were increased in the PBMCs of patients with SLE compared with healthy control subjects, whereas there were no significant differences in the percentages of IL-22-positive CD8+ T cells. There was a strong positive correlation between the proportion of CD4+ T cells expressing IL-22 and SLEDAI score (r (s) = 0.65, P < 0.001). Furthermore, the frequencies of IL-22-positive CD4+ T cells were significantly higher in patients with SLE with nephritis than those without nephritis (Z = -2.72, P < 0.01). In conclusion, increased frequencies of IL-22-positive CD4+ T cells in patients with SLE and positive correlation with SLEDAI score and lupus nephritis suggest that this cytokine may be implicated in the pathogenesis of the disease.

Indexed as

AdultCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleFlow CytometryHumansInterleukin-22InterleukinsLeukocytes, MononuclearLupus Erythematosus, SystemicLupus NephritisMaleMiddle AgedInterleukin-22Interleukins

Identifiers

PMID21487830
OpenAlexW2043423708

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Read underepoch 390

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.