Evidence map›Paper›PMID 18462346›Full record

ArticleImmunology2008

The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cells.

Jeremy D Isaacs, Oliver A Garden, Gurman Kaur, John Collinge, Graham S Jackson, Daniel M Altmann

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. A genome-wide association study on African-ancestry populations for asthma.The Journal of allergy and clinical immunology · 2010
    Pooled it
  2. Review
  3. The multiple functions of PrPJournal of molecular medicine (Berlin, Germany) · 2022
    Review
  4. Article
  5. Article
  6. Immuno-Navigator, a batch-corrected coexpression database, reveals cell type-specific gene networks in the immune system.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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 4 institutions in 1 country.

Jeremy D IsaacsDepartment of Infectious Diseases and Immunity, Imperial College, Hammersmith Hospital, London, UK.
Oliver A Garden
Gurman Kaur
John Collinge
Graham S Jackson
Daniel M Altmann
Hammersmith Hospital · GBUniversity College London · GBImperial College London · GBMRC Prion Unit · GB

Funding

Medical Research Council G0700153Medical Research Council MC_U123170362Medical Research Council MC_U123192748Wellcome Trust
6 · The paper itself

Abstract

Post-translational modification of the cellular prion protein (PrP(C)) is intimately associated with the pathogenesis of prion disease, yet the normal function of the protein remains unclear. PrP(C) is expressed in lymphoid cells and is known to be a T-cell activation antigen. Further, transcription profiling studies of regulatory T cells have shown preferential overexpression of PrP(C), suggesting a possible role in regulatory function. We report that both the expression of PrP message and cell surface PrP(C) levels are increased in murine CD4(+) CD25(+) regulatory T cells compared with CD4(+) CD25(-) cells. However, PrP(0/0) mice do not show altered regulatory T-cell numbers or forkhead box P3 (Foxp3) expression levels, or impaired regulatory T-cell function in vitro. Nevertheless, the preferential expression of surface PrP(C) by regulatory T cells raises the possibility that therapeutic ligation of PrP(C) might alter immune regulation.

Indexed as

AnimalsCells, CulturedForkhead Transcription FactorsImmune ToleranceInterleukin-2 Receptor alpha SubunitMiceMice, Inbred C57BLPrPC ProteinsReverse Transcriptase Polymerase Chain ReactionT-Lymphocytes, RegulatoryUp-RegulationForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2 Receptor alpha SubunitPrPC Proteins

Identifiers

PMID18462346
PMCPMC2669135
OpenAlexW1978028430

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.