Evidence map›Paper›PMID 30809737›Full record

ArticleClinical rheumatology2019

Elevated circulating T cell subsets and cytokines expression in patients with rheumatoid arthritis.

Haiyan Zhou, Bailong Hu, Zheng Zhaopeng, Jun Liu, Qin Zhong, Youyang Fan, Long Li

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. MCP-1: Function, regulation, and involvement in disease.International immunopharmacology · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Skeletal muscle redox signaling in rheumatoid arthritis.Clinical science (London, England : 1979) · 2020
    Review
  13. Article
  14. 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

7 authors at 2 institutions in 1 country.

Haiyan Zhou *Department of Clinical Research Centre, The Affiliated Hospital of Guizhou Medical University, 550004, Guiyang, 550004, Guizhou Province, People's Republic of China. zhouhaiyan12388@126.com.
Bailong Hu *Department of Anesthesiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, Guizhou Province, People's Republic of China.
Zheng Zhaopeng *Guizhou Medical University, Guiyang, 550004, Guizhou Province, People's Republic of China.
Jun LiuDepartment of Immunology and Rheumatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, Guizhou Province, People's Republic of China.
Qin ZhongDepartment of Clinical Research Centre, The Affiliated Hospital of Guizhou Medical University, 550004, Guiyang, 550004, Guizhou Province, People's Republic of China.
Youyang FanDepartment of Immunology and Rheumatology, The Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, Guizhou Province, People's Republic of China.
Long LiDepartment of Immunology and Rheumatology, The Third Affiliated Hospital of Guizhou Medical University, Guiyang, 550004, Guizhou Province, People's Republic of China. gzyxyll@medmail.com.
Guiyang Medical University · CNAffiliated Hospital of Guizhou Medical University · CN

Funding

Fund of Guiyang Science and Technology department [2017]30-10Fund of Qiannan Science and Technology department qiannankeheshezi[2017]73National Natural Science Foundation of China 81460254Population and Family Planning Commission of Shandong Province (CN) gzwjkj2017-1-016the Science and Technology Fund of Guizhou Provincial Health Department qiankehejichu[2018]1137
6 · The paper itself

Abstract

objectiveThis study aimed to assess the role of different subsets of circulating follicular helper T cells (Tfh), central memory (TCM), effector memory (TEM), Naïve T, chemokines, and cytokines in the pathogenesis of rheumatoid arthritis (RA).

methodsBlood samples from RA patients (n = 44) and healthy controls (n = 37) were analyzed. The frequencies of circulating Tfh, TCM, TEM, and Naïve T cell subsets were enumerated, and the expression of co-stimulatory molecules, such as inducible co-stimulator (ICOS) and programmed death-1 (PD1), on these cells was evaluated by flow cytometry. The disease state in RA patients was assessed using the DAS28. Concentrations of C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), anti-cyclic citrullinated peptide (anti-CCP), and rheumatoid factor (RF) were measured. Cytokines and chemokines, such as IL-1β, TNF-α, IL-4, IL-6, IL-9, IL-17A, MCP-1, IL-10, IL-12p70, and IL-21, were measured by a cytometric beads array assay.

resultsThe percentages of circulating PD1

conclusionsElevated circulating T cell subsets and cytokines expression profile were observed in RA patients. IL-6, MCP-1, and IL-1β were significantly increased in RA, and PD1

Indexed as

AdolescentAdultArthritis, RheumatoidAutoantibodiesBlood SedimentationCase-Control StudiesChemokinesC-Reactive ProteinCross-Sectional StudiesCytokinesFemaleHumansLymphocyte CountMaleMiddle AgedT-Lymphocytes, Helper-InducerAutoantibodiesChemokinesC-Reactive ProteinCytokinesFollicular help T cellsMemory T cellsRheumatoid arthritis

Identifiers

PMID30809737
OpenAlexW2916725304

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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.