Evidence map›Paper›PMID 18993084›Full record

ArticleImmunity2008

CD4+CD25+ regulatory T cells suppress mast cell degranulation and allergic responses through OX40-OX40L interaction.

Giorgia Gri, Silvia Piconese, Barbara Frossi, Vanessa Manfroi, Sonia Merluzzi, Claudio Tripodo, Antonella Viola, Sandra Odom, Juan Rivera, Mario P Colombo and 1 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

178 citing papers in PubMed, 385 citations in OpenAlex.

  1. Trial
  2. Review
  3. OX40/OX40L modulation: A target for regulating T cells in cutaneous inflammatory disorders.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Review
  4. Review
  5. Article
  6. Integrated multi-omics and machine learning prioritize key immune genes for multiple sclerosis risk prediction.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. T Regulatory Mechanisms in Airway and Interstitial Lung Disease.Seminars in respiratory and critical care medicine · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Giorgia GriDepartment of Biomedical Science and Technology, University of Udine, 33100 Udine, Italy.
Silvia Piconese
Barbara Frossi
Vanessa Manfroi
Sonia Merluzzi
Claudio Tripodo
Antonella Viola
Sandra Odom
Juan Rivera
Mario P Colombo
Carlo E Pucillo
University of Udine · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USUniversity of Padua · ITUniversity of Palermo · IT

Funding

Role of Mast Cells in Immunity and AutoimmunityZIAAR041156 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI RIVERA, JUAN · 2009 to 2013
$6.8M
Molecular Regulation of InflammationZIAAR041155 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI RIVERA, JUAN · 2009 to 2013
$5.0M
Role of Mast Cells in Immunity and AutoimmunityZ01AR041156 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI RIVERA, JUAN · 2007 to 2008
$2.0M
Intramural NIH HHS Z01 AR041156
6 · The paper itself

Abstract

T regulatory (Treg) cells play a role in the suppression of immune responses, thus serving to induce tolerance and control autoimmunity. Here, we explored whether Treg cells influence the immediate hypersensitivity response of mast cells (MCs). Treg cells directly inhibited the FcvarepsilonRI-dependent MC degranulation through cell-cell contact involving OX40-OX40L interactions between Treg cells and MCs, respectively. When activated in the presence of Treg cells, MCs showed increased cyclic adenosine monophosphate (cAMP) concentrations and reduced Ca(2+) influx, independently of phospholipase C (PLC)-gamma2 or Ca(2+) release from intracellular stores. Antagonism of cAMP in MCs reversed the inhibitory effects of Treg cells, restoring normal Ca(2+) responses and degranulation. Importantly, the in vivo depletion or inactivation of Treg cells caused enhancement of the anaphylactic response. The demonstrated crosstalk between Treg cells and MCs defines a previously unrecognized mechanism controlling MC degranulation. Loss of this interaction may contribute to the severity of allergic responses.

Indexed as

Cell DegranulationAnimalsCalciumCell Line, TumorGene Knockdown TechniquesHistamine ReleaseHumansHypersensitivityMast CellsMembrane GlycoproteinsMiceMice, Inbred BALB CMice, Inbred C57BLOX40 LigandPhospholipase C gammaReceptors, OX40CalciumMembrane GlycoproteinsOX40 LigandPhospholipase C gammaReceptors, OX40Tnfrsf4 protein, mouseTnfsf4 protein, mouseTumor Necrosis Factors

Identifiers

PMID18993084
PMCPMC2590499
OpenAlexW2035023446

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.