Evidence map›Paper›PMID 23954573›Full record

ArticleClinical immunology (Orlando, Fla.)2013

Psoriasis patients exhibit impairment of the high potency CCR5(+) T regulatory cell subset.

David C Soler, Hideaki Sugiyama, Andrew B Young, Jessica V Massari, Thomas S McCormick, Kevin D Cooper

Open access · hybridAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Cellular Mechanisms of Psoriasis Pathogenesis: A Systemic Review.Clinical, cosmetic and investigational dermatology · 2023
    Review
  7. Article
  8. Article
  9. Ferroptosis: Mechanism and connections with cutaneous diseases.Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Review
  12. Article
  13. [Genetically modified regulatory T cells: therapeutic concepts and regulatory aspects].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2020
    Review
  14. Regulatory T Cell Plasticity and Stability and Autoimmune Diseases.Clinical reviews in allergy & immunology · 2020
    Review
  15. Advances in Understanding the Immunological Pathways in Psoriasis.International journal of molecular sciences · 2019
    Review
  16. Regulatory T cells in the treatment of disease.Nature reviews. Drug discovery · 2018
    Review
  17. Review
  18. The ratio of HLA-DR and VNN2Journal of neuro-oncology · 2017
    Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

David C SolerDepartment of Dermatology, Case Western Reserve University, Cleveland, OH 44106, USA; The Murdough Family Center for Psoriasis, University Hospitals Case Medical Center, Cleveland, OH 44106, USA.
Hideaki Sugiyama
Andrew B Young
Jessica V Massari
Thomas S McCormick
Kevin D Cooper
Case Western Reserve University · USSeirei Hamamatsu General Hospital · JPUniversity Hospitals Case Medical Center · US

Funding

Vitamin D endocrine system and Protection Against Skin TumorlgenesisP30AR039750 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI COOPER, KEVIN D · 1988 to 2015
$9.1M
Systems Biology CoreP50AR055508 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI DIAZ-INSUA, MIREYA · 2007 to 2011
$6.8M
Psoriatic Regulatory T cell DysfunctionR01AR051498 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI COOPER, KEVIN D · 2004 to 2014
$3.5M
NIAMS NIH HHS P30 AR039750NIAMS NIH HHS P30AR039750NIAMS NIH HHS P50 AR055508NIAMS NIH HHS P50AR055508NIAMS NIH HHS R01 AR051498NIAMS NIH HHS R01AR051498
6 · The paper itself

Abstract

CCR5 expression on CD4(+)CD25(high)Foxp3(+) regulatory T cells (Tregs) has been reported to be crucial for limiting Th1 inflammation associated with autoimmunity and bacterial infections. We inquired whether abnormalities in chemokine receptors expressed on Tregs might be involved in the psoriatic pathogenesis. Indeed, the proportion of CCR5(+) Treg was 58.8% in healthy individuals (n=9), whereas only half as many CCR5(+) Treg cells were found in psoriatic individuals (29.1%, n=8, p<0.01). The flow-enriched control CCR5(+) Tregs consistently exceeded the suppressive capacity of unsorted Tregs in autologous MLR assays (n=5, p<0.05) showing that CCR5(+) Treg subset is a high potency regulatory T cell population. Interestingly, psoriatic CCR5(+) Treg cells exhibited significantly less migratory capacity toward CCR5 ligands MIP-1β and RANTES in vitro compared to CCR5(+) Treg controls (n=3, p<0.05). Our data demonstrate that psoriatic CCR5(+) Tregs cells are numerically-, functionally- and chemotactically-deficient compared to controls and may pose a triple impairment on the ability of psoriatic Tregs to restrain inflammation.

Indexed as

Adaptor Proteins, Signal TransducingAdultChemokine CCL5ChemotaxisHumansPsoriasisReceptors, CCR5T-Lymphocytes, RegulatoryAdaptor Proteins, Signal TransducingCCL5 protein, humanChemokine CCL5MAPKAP1 protein, humanReceptors, CCR5ImmunosuppressionPsoriasisRegulatory T cells

Identifiers

PMID23954573
PMCPMC3854939
OpenAlexW2081008140

What OpenQuestion holds

Textmetadata
LicenceTDM
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.