Evidence map›Paper›PMID 16236126›Full record

ArticleImmunology2005

Induction of antigen-specific regulatory T cells in the liver-draining celiac lymph node following oral antigen administration.

Susanne Hultkrantz, Sofia Ostman, Esbjörn Telemo

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Dynamics of antigen presentation to transgene product-specific CD4Molecular therapy. Methods & clinical development · 2016
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Oral tolerance.Immunological reviews · 2011
    Review
  14. Review
  15. Article
  16. Article
  17. Oral tolerance.Immunological reviews · 2005
    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

3 authors at 1 institution in 1 country.

Susanne HultkrantzDepartment of Rheumatology and Inflammation Research, University of Göteborg, Göteborg, Sweden.
Sofia Ostman
Esbjörn Telemo
University of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells are induced by oral administration of an antigen, but the physiological requirements and localization of the inductive sites are largely unknown. Using an adoptive transfer system of cells transgenic for ovalbumin T-cell receptor (OVA TCR tg), we found that antigen-specific CD4+ T cells were activated in the liver-draining celiac lymph node (CLN) shortly after ovalbumin feeding, and that a significantly higher proportion of the T cells in the CLN developed into the putative regulatory phenotype [co-expressing CD25 with the glucocortico-induced tumour necrosis factor (TNF) receptor family related gene (GITR), cytotoxic T-lymphocyte antigen (CTLA)-4 and CD103] than in Peyer's patches, the mesenteric and peripheral lymph nodes and the spleen. In addition, a particularly high level of expression of CD103 on the OVA-specific T cells in the CLN may favour homing to the epithelium of the intestine. While equally suppressive, OVA tg T cells isolated from the CLN of OVA-fed DO11.10 mice were less dependent on transforming growth factor (TGF)-beta for suppression than cells isolated from the peripheral and mesenteric lymph nodes, which indicates the involvement of an additional suppressive mechanism. The expression of FoxP3 was not up-regulated in any of the lymph node compartments studied. Our phenotypic and functional findings suggest that the induction of regulatory T cells in the CLN may be relevant in the control of the immune response to dietary antigens.

Indexed as

Administration, OralAdoptive TransferAnimalsAntigens, CDAntigens, DifferentiationCD4-Positive T-LymphocytesCeliac ArteryCTLA-4 AntigenEpitopes, T-LymphocyteFemaleFlow CytometryForkhead Transcription FactorsGlucocorticoid-Induced TNFR-Related ProteinImmune ToleranceImmunity, MucosalImmunophenotypingalpha E integrinsAntigens, CDAntigens, DifferentiationCTLA-4 AntigenCtla4 protein, mouseEpitopes, T-LymphocyteForkhead Transcription FactorsFoxp3 protein, mouseGlucocorticoid-Induced TNFR-Related ProteinIntegrin alpha ChainsOvalbuminProteinsReceptors, Interleukin-2Receptors, Nerve Growth FactorReceptors, Tumor Necrosis FactorTnfrsf18 protein, mouse

Identifiers

PMID16236126
PMCPMC1802428
OpenAlexW2086456032

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.