Evidence map›Paper›PMID 26436101›Full record

ArticleJournal of immunology research2015

The Clinical Relevance of IL-17-Producing CD4+CD161+ Cell and Its Subpopulations in Primary Sjögren's Syndrome.

Linbo Li, Jing He, Lei Zhu, Yuqin Yang, Yuebo Jin, Rulin Jia, Xu Liu, Yanying Liu, Xiaolin Sun, Zhanguo Li

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2015. 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
1.1field-weighted citation impact, top 21% 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, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The proportion of CD161 on CD56Immunity, inflammation and disease · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. CD147-mediated chemotaxis of CD4Clinical rheumatology · 2018
    Article
  12. 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

10 authors at 1 institution in 1 country.

Linbo LiDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Jing HeDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Lei ZhuDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Yuqin YangDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Yuebo JinDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Rulin JiaDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Xu LiuDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Yanying LiuDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Xiaolin SunDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Zhanguo LiDepartment of Rheumatology & Immunology, Clinical Immunology Center, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTh17 cells have been demonstrated to play an important role in the onset and development of primary Sjögren's syndrome (pSS). In this study, we evaluated the expansion and clinical significance of circulating CD4+CD161+ T cell and its "effector" (CD4+CD25-CD161+ T cell) and "regulatory" (CD4+CD25+CD161+ T cell) subpopulations.

methodsFifty-eight pSS patients and 16 healthy controls (HCs) were recruited in our study. The cell populations and intracellular IL-17 expression were analyzed by flow cytometry. The disease activity was evaluated by the EULAR-SS Disease Activity Index (ESSDAI). Autoantibodies were measured by ELISA or indirect immunofluorescence assay.

resultsThe CD161+ T cell fractions showed higher proportions of IL-17-producing cells. The frequencies of the overall CD4+CD161+ T cell population and its effector subset were positively correlated with disease activity parameters and more severe disease manifestations. A significant elevation of the CD4+CD25+CD161+ T cell subpopulation was observed in the peripheral blood of pSS patients compared to HCs and this subset showed decreased regulatory functions compared with the CD4+CD25+CD161- population.

conclusionCirculating CD4+CD161+ T cell populations associated with pSS disease activity and severity. These cells might be involved in the development of pSS and could be potential therapeutic targets in the treatment of pSS.

Indexed as

AdultAgedBiomarkersCase-Control StudiesCD4 Lymphocyte CountCytokinesFemaleFlow CytometryHumansImmunophenotypingInterleukin-17MaleMiddle AgedNK Cell Lectin-Like Receptor Subfamily BSjogren's SyndromeTh17 CellsBiomarkersCytokinesInterleukin-17NK Cell Lectin-Like Receptor Subfamily B

Identifiers

PMID26436101
PMCPMC4578753
OpenAlexW2397877020

What OpenQuestion holds

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LicenceCC BY
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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.