Evidence map›Paper›PMID 18521187›Full record

ArticleThe Journal of clinical investigation2008

TGF-beta-dependent suppressive function of Tregs requires wild-type levels of CD18 in a mouse model of psoriasis.

Honglin Wang, Thorsten Peters, Anca Sindrilaru, Daniel Kess, Tsvetelina Oreshkova, Xue-Zhong Yu, Anne Maria Seier, Heike Schreiber, Meinhard Wlaschek, Robert Blakytny and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. T-Cell Adhesion in Healthy and Inflamed Skin.JID innovations : skin science from molecules to population health · 2021
    Review
  7. Review
  8. The Role of Helper T Cells in Psoriasis.Frontiers in immunology · 2021
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Scanning the Immunopathogenesis of Psoriasis.International journal of molecular sciences · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. The Inflammatory Response in Psoriasis: a Comprehensive Review.Clinical reviews in allergy & immunology · 2016
    Review
  19. GP96 is a GARP chaperone and controls regulatory T cell functions.The Journal of clinical investigation · 2015
    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

14 authors at 2 institutions in 2 countries.

Honglin WangDepartment of Dermatology and Allergic Diseases, University of Ulm, Ulm, Germany.
Thorsten Peters
Anca Sindrilaru
Daniel Kess
Tsvetelina Oreshkova
Xue-Zhong Yu
Anne Maria Seier
Heike Schreiber
Meinhard Wlaschek
Robert Blakytny
Jan Röhrbein
Guido Schulz
Johannes M Weiss
Karin Scharffetter-Kochanek
Universität Ulm · DEMoffitt Cancer Center · US

Funding

Effects of Foxp3-Induced Regulatory T Cells on GVHD and GVT ActivityR01CA118116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2006 to 2015
$2.2M
Control of GVHD by Inducible T-Regulatory CellsR21AI063553 · NIAID · H. LEE MOFFITT CANCER CTR &RES INST · PI YU, XUE-ZHONG · 2005 to 2005
$243k
NCI NIH HHS CA-118116NCI NIH HHS R01 CA118116NIAID NIH HHS AI-063553NIAID NIH HHS R21 AI063553
6 · The paper itself

Abstract

Dysfunctional Tregs have been identified in individuals with psoriasis. However, their role in the pathogenesis of the disease remains unclear. Here we explored the effect of diminished CD18 (beta2 integrin) expression on the function of CD4+CD25+CD127(-) Tregs using the Cd18 hypomorphic (Cd18hypo) PL/J mouse model of psoriasis that closely resembles the human disease. We found that reduced CD18 expression impaired cell-cell contact between Tregs and DCs. This led to dysfunctional Tregs, which both failed to suppress the pathogenic T cells and promoted the onset and severity of the disease. This failure was TGF-beta-dependent, as Tregs derived from Cd18hypo PL/J mice had diminished TGF-beta1 expression. Adoptive transfer of Tregs expressing wild-type levels of CD18 into affected Cd18hypo PL/J mice resulted in a substantial improvement of the psoriasiform skin disease, which did not occur upon coinjection of the cells with TGF-beta-specific neutralizing antibody. Our data indicate a primary dysfunction of Cd18hypo Tregs, allowing subsequent hyperproliferation of pathogenic T cells in the Cd18hypo PL/J mouse model of psoriasis. This study may provide a step forward in our understanding of the unique role of CD18 expression levels in avoiding autoimmunity.

Indexed as

Adoptive TransferAnimalsAnimal StructuresAntibodiesCD18 AntigensCD4 Lymphocyte CountCD4-Positive T-LymphocytesCell CommunicationCell ProliferationDendritic CellsDisease Models, AnimalLymphocyte ActivationLymphocyte Culture Test, MixedMiceMice, Inbred C57BLMice, Inbred StrainsAntibodiesCD18 AntigensTransforming Growth Factor beta1

Identifiers

PMID18521187
PMCPMC2398739
OpenAlexW2020014005

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.