Evidence map›Paper›PMID 25663558›Full record

ArticleInflammation2015

Analysis of Programmed Death-1 in Patients with Psoriatic Arthritis.

Michael Peled, Marianne Strazza, Inbar Azoulay-Alfaguter, Gregg J Silverman, Jose U Scher, Adam Mor

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Imbalance of T Lymphocyte Subsets in Adult Immune Thrombocytopenia.International journal of general medicine · 2021
    Article
  10. Article
  11. Article
  12. [Initially undetected de novo psoriasis triggered by nivolumab for metastatic base of the tongue carcinoma].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2018
    Article
  13. Percentages of PD-1Human vaccines & immunotherapeutics · 2018
    Article
  14. Article
  15. Review
  16. The Potential Role of Inhibitory Receptors in the Treatment of Psoriasis.Bulletin of the Hospital for Joint Disease (2013) · 2017
    Review
  17. Suppressed Programmed Death 1 Expression on CD4Mediators of inflammation · 2017
    Article
  18. Review
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Michael PeledThe Department of Medicine, New York University School of Medicine, 450 E 29th Street, New York, NY, 10016, USA.
Marianne Strazza
Inbar Azoulay-Alfaguter
Gregg J Silverman
Jose U Scher
Adam Mor
New York University · US

Funding

The Role of Gut and Skin Microbiome in Psoriatic ArthritisK23AR064318 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHER, JOSE U. · 2013 to 2016
$589k
NIAMS NIH HHS K23 AR064318
6 · The paper itself

Abstract

Programmed death-1 (PD-1) is an inhibitory co-receptor that is highly expressed in T lymphocytes that has been shown to downregulate inflammatory responses in several inflammatory diseases including systemic lupus erythematosus and rheumatoid arthritis. Yet, the role of PD-1 in psoriatic arthritis (PsA) has not been studied. In order to fill this gap, we measured the expression levels of PD-1 in peripheral T cells from patients with active disease. Twenty patients and fifteen age-matched healthy control subjects were recruited. The percentage of CD3(+)PD-1(+) T cells was measured by flow cytometry. Despite normal concentration of peripheral T cells, the expression levels of PD-1 were significantly higher in patients compared to healthy controls. Interestingly, among the patients, the expression levels inversely correlated with disease activity measured by disease activity scores (DAS28). PD-1 expression levels strongly correlated with the number of tender and swollen joints, but not with C-reactive protein (CRP) levels or psoriasis area and severity index (PASI). Functionally, in vitro ligation of PD-1 receptor in PsA T cells inhibited interleukin-2 (IL-2) secretion, Akt phosphorylation, and Rap1 activation. These findings suggest that PD-1 might serve as a biomarker for disease activity in PsA and highlight the need for additional studies in order to establish the role of PD-1 in PsA pathogenesis.

Indexed as

AdultAgedArthritis, PsoriaticBiomarkersCase-Control StudiesCells, CulturedFemaleHumansMaleMiddle AgedProgrammed Cell Death 1 ReceptorYoung AdultBiomarkersPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID25663558
OpenAlexW2032669080

What OpenQuestion holds

Textmetadata
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.