Evidence map›Paper›PMID 21908737›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Peroxisome proliferator-activated receptor gamma is required for CD4+ T cell-mediated lymphopenia-associated autoimmunity.

William J Housley, Catherine O Adams, Amanda G Vang, Stefan Brocke, Frank C Nichols, Melissa LaCombe, Thiruchandurai V Rajan, Robert B Clark

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Nutrients: Signal 4 in T cell immunity.The Journal of experimental medicine · 2024
    Article
  3. Review
  4. Review
  5. Review
  6. Sex-specific regulation of immune responses by PPARs.Experimental & molecular medicine · 2017
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Autoimmunity in 2012.Clinical reviews in allergy & immunology · 2013
    Review
  16. Metabolic control of the Treg/Th17 axis.Immunological reviews · 2013
    Review
  17. Article
  18. Review
  19. Autoimmunity in 2011.Clinical reviews in allergy & immunology · 2012
    Review
  20. Review
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

8 authors at 1 institution in 1 country.

William J HousleyCenter for Immunotherapy of Cancer and Infectious Diseases, University of Connecticut Health Center, Farmington, CT 06032, USA.
Catherine O Adams
Amanda G Vang
Stefan Brocke
Frank C Nichols
Melissa LaCombe
Thiruchandurai V Rajan
Robert B Clark
UConn Health · US

Funding

BASIC IMMUNOLOGY &IMMUNOLOGIC CELL INJURYT32AI007080 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ADLER, ADAM J, VELLA, ANTHONY T · 1985 to 2012
$1.4M
The Role of PPARGamma in the Generation and Function of TregsR56AI072533 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CLARK, ROBERT BENNETT · 2007 to 2007
$357k
NIAID NIH HHS 2T32AI007080NIAID NIH HHS IR56 AI072533-01 A1NIAID NIH HHS R56 AI072533NIAID NIH HHS T32 AI007080
6 · The paper itself

Abstract

The nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ) was shown to play an immunoregulatory role in many immune-related cell types, and activation of PPARγ was reported to be an effective therapeutic approach in murine and human autoimmune disease. However, despite an association between lymphopenia and autoimmunity, there has been no study on the role of T cell PPARγ in lymphopenia-associated autoimmunity. In the present studies, we examined the role of PPARγ in CD4(+) T cells in two murine models of lymphopenia-associated autoimmunity. Surprisingly, we found that PPARγ expression in CD4(+) CD25(-) T cells (T effector cells [Teffs]) is actually required for development of autoimmunity under lymphopenic conditions. Mechanistically, the inability of PPARγ-deficient (T-PPAR) Teffs to mediate lymphopenic autoimmunity is associated with a significant decrease in accumulation of Teffs in the spleen, lymph nodes, and tissues after adoptive transfer. This abnormal accumulation of T-PPAR Teffs was associated with defects in both in vivo proliferation and survival. Additionally, T-PPAR Teffs demonstrated decreased cytokine production in inflammatory sites and decreased expression of the homing receptor α4β7. Finally, these abnormalities in T-PPAR Teff function were not elicited by lymphopenia alone but also required the additional activation involved in the mediation of autoimmunity. Thus, in contrast to its documented immunosuppressive role, we identified an unexpected function for PPARγ in Teffs: a role in Teff proliferation and survival in lymphopenia-associated autoimmunity. These findings highlight both the multifunctional role of PPARγ in T cells and the complexity of PPARγ as a potential therapeutic target in autoimmunity.

Indexed as

Adoptive TransferAnimalsApoptosisAutoimmunityCD4-Positive T-LymphocytesCell ProliferationCell SeparationCytokinesFemaleFlow CytometryLymphopeniaMiceMice, KnockoutPPAR gammaCytokinesPPAR gamma

Identifiers

PMID21908737
PMCPMC3189448
OpenAlexW2102830399

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.