Evidence map›Paper›PMID 27065298›Full record

ArticleMediators of inflammation2016

Circulating Angiogenic T Cells and Their Subpopulations in Patients with Systemic Lupus Erythematosus.

Jinlin Miao, Feng Qiu, Tingting Li, Peng Zhao, Kui Zhang, Minghua Lv, Jun Wan, Xiaokun Qi, Ping Zhu

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Cardiovascular disease in systemic lupus erythematosus.Rheumatology and immunology research · 2021
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Circulating Angiogenic T Cells Are Increased in Lupus Nephritis Patients.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Observational
  18. Review
  19. 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

9 authors at 4 institutions in 1 country.

Jinlin MiaoDepartment of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Feng QiuDepartment of Neurology, Chinese Navy General Hospital, Beijing 100048, China.
Tingting LiDepartment of Geriatric Gastroenterology, Chinese People's Liberation Army General Hospital, Beijing 100853, China.
Peng ZhaoDepartment of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China; Department of Hematology and Rheumatology, Hanzhong 3201 Hospital, Medicine School of Xi'an Jiaotong University, Hanzhong 723000, China.
Kui ZhangDepartment of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Minghua LvDepartment of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Jun WanDepartment of Geriatric Gastroenterology, Chinese People's Liberation Army General Hospital, Beijing 100853, China.
Xiaokun QiDepartment of Neurology, Chinese Navy General Hospital, Beijing 100048, China.
Ping ZhuDepartment of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Xijing Hospital · CNChinese People's Liberation Army · CNPLA Navy General Hospital · CNHanzhong People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSystemic lupus erythematosus (SLE) is associated with accelerated atherosclerosis and increased cardiovascular risk. Angiogenic T cells (Tang), a specific T cell subset, have been identified and involved in the repair of damaged endothelium. This study aimed to analyze the Tang cell subsets in relation to disease specific features from SLE patients.

methodsTang cell subsets were assessed in peripheral blood samples from 41 SLE patients and 22 healthy controls (HC) by flow cytometry on the basis of CD31 and CXCR4 expression on CD3+, CD4+, and CD8+ T cells.

resultsThe percentage of circulating CD8+CD31+CXCR4+ T cells (CD8+ Tang), but not CD3+CD31+CXCR4+ T cells (Tang) and CD4+CD31+CXCR4+ T cells (CD4+ Tang), in SLE was higher than HC. The percentages of Tang cell subsets in anti-dsDNA-positive SLE patients were significantly increased as compared to their negative counterparts and HC. Additionally, the levels of circulating Tang cell subsets were negatively correlated with age at sampling and at diagnosis, but not disease duration or disease activity.

conclusionAnti-dsDNA-positivity may identify a group of SLE patients with increased Tang cell subsets and circulating CD8+ Tang cells may be viewed as a potentially useful biomarker of endothelial damage and cardiovascular risk in SLE.

Indexed as

AdultCD3 ComplexCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleFlow CytometryHumansLupus Erythematosus, SystemicMaleT-Lymphocyte SubsetsYoung AdultCD3 Complex

Identifiers

PMID27065298
PMCPMC4811166
OpenAlexW2302140953

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.