Evidence map›Paper›PMID 26608464›Full record

ArticleArthritis research & therapy2015

Soluble PD-1 aggravates progression of collagen-induced arthritis through Th1 and Th17 pathways.

Cuiping Liu, Juean Jiang, Li Gao, Xiaoting Wang, Xiaohan Hu, Min Wu, Jian Wu, Ting Xu, Qin Shi, Xueguang Zhang

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 4% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Matrix Type Influences the Levels of Soluble Immune Checkpoints.Journal of clinical laboratory analysis · 2026
    Article
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  14. Surface PD-1 expression in T cells is suppressed by HNRNPK through an exonic splicing silencer on exon 3.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  15. Article
  16. Article
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  18. Article
  19. Characteristics of PD-1Clinical & translational immunology · 2024
    Article
  20. Review

6 more citing papers are in PubMed but not listed here.

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.

Cuiping LiuJiangsu Institute of Clinical Immunology, First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Juean JiangJiangsu Institute of Clinical Immunology, First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Li GaoJiangsu Province Key Laboratory of Stem Cell Research, Soochow University, Suzhou, 215006, China.
Xiaoting WangJiangsu Province Key Laboratory of Stem Cell Research, Soochow University, Suzhou, 215006, China.
Xiaohan HuJiangsu Province Key Laboratory of Stem Cell Research, Soochow University, Suzhou, 215006, China.
Min WuDepartment of Rheumatology, Third Affiliated Hospital of Soochow University, Changzhou, 213003, China.
Jian WuJiangsu Institute of Clinical Immunology, First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Ting XuDepartment of Rheumatology, Third Affiliated Hospital of Soochow University, Changzhou, 213003, China.
Qin ShiJiangsu Institute of Clinical Immunology, First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Xueguang ZhangJiangsu Institute of Clinical Immunology, First Affiliated Hospital of Soochow University, Suzhou, 215006, China. xueguangzh@126.com.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe programmed cell death 1 (PD-1) protein is a critical regulator of T-cell activation and is also an important therapeutic target for autoimmune diseases. Little is known about the regulation and functional properties of the soluble PD-1 (sPD-1) variant. The aim of this study was to examine the role of sPD-1 in the regulation of human and murine rheumatoid arthritis (RA).

methodsExpression of cytokines and sPD-1 in sera, synovial fluid, and peripheral blood (PB) mononuclear cells of patients with RA were analyzed by enzyme-linked immunosorbent assay and quantitative polymerase chain reaction. PD-1 function was assessed in PB T cells after stimulation of the cells with anti-CD3 and PD-L1-Fc to crosslink PD-1. Recombinant PD-1-Fc was injected intraperitoneally into DBA/1 mice with collagen-induced arthritis (CIA) to analyze the function of sPD-1 in vivo.

resultsHigh concentrations of sPD-1 were found in sera and synovial fluid of patients with RA. The levels of serum sPD-1 were significantly correlated with titers of rheumatoid factor (RF) (r = 0.306, p = 0.005) and 28-joint Disease Activity Score (r = 0.545, p < 0.001). Further characterization of sPD-1 revealed that it functionally blocked the inhibitory effect of membrane-bound PD-1 on T-cell activation. Interferon γ, tumor necrosis factor α, and interleukin 17A were identified as inducers of sPD-1 in vitro. Moreover, PD-1-Fc enhanced proinflammatory cytokine expression, generation of Th1 cells and Th17 cells, and joint pathology in a CIA model.

conclusionssPD-1 regulates peripheral T-cell responses in both human and murine RA. Thus, sPD-1 may represent an additional biomarker or target in immunomodulatory therapy for RA.

Indexed as

AdultAgedAnimalsArthritis, ExperimentalArthritis, RheumatoidDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansLymphocyte ActivationMaleMiceMice, Inbred DBAMiddle AgedProgrammed Cell Death 1 ReceptorPDCD1 protein, humanPdcd1 protein, mouseProgrammed Cell Death 1 Receptor

Identifiers

PMID26608464
PMCPMC4659197
OpenAlexW2178033498

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.