Evidence map›Paper›PMID 19476512›Full record

ReviewImmunology2009

Endosomal processing for antigen presentation mediated by CD1 and Class I major histocompatibility complex: roads to display or destruction.

Marianne Boes, Arie J Stoppelenburg, Fenna C M Sillé

Open access · greenAbstract readReview
In one paragraph

Review in Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. 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 3 institutions in 2 countries.

Marianne BoesDepartment of Pediatric Immunology, University Medical Center Utrecht, Wilhelmina Children's Hospital, the Netherlands. mboes@umcutrecht.nl
Arie J Stoppelenburg
Fenna C M Sillé
Harvard University · USUniversity Medical Center Utrecht · NLWilhelmina Children's Hospital · NL

Funding

Class II MHC & CD1d antigen presentation pathways in skin-derived dendritic cellsR01AR052810 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI FUHLBRIGGE, ROBERT C · 2007 to 2011
$1.0M
NIAMS NIH HHS R01 AR052810
6 · The paper itself

Abstract

The presentation of antigen in a form that can be recognized by T lymphocytes of the immune system requires antigen processing and association of antigen-derived fragments with molecules encoded by the major histocompatibility complex (MHC) locus or by the CD1 locus. Much emphasis on antigen processing and presentation in the last decades has focused on what we consider 'conventional routes' of antigen processing and presentation, whereby extracellular antigens are processed for presentation via Class II MHC complexes and cytosolic antigens are presented as peptide-Class I MHC complexes. We here highlight two other pathways in myeloid dendritic cells, those of lipid antigen presentation in association with CD1 and of peptide cross-presentation via Class I MHC complexes. Some pathogens evade immune recognition through inhibition of antigen presentation of phagosomal origin. Deviations in endosomal antigen processing and presentation are also seen in individuals suffering from glycosphingolipid lysosomal lipid storage diseases. We summarize recent developments in the endosomal antigen processing and presentation pathway, for display as lipid-CD1 complexes to natural killer T cells and as peptide-Class I MHC complexes to CD8 T cells.

Indexed as

AnimalsAntigen PresentationAntigens, CD1Bacterial InfectionsDendritic CellsEndosomesGenetic Diseases, InbornHistocompatibility Antigens Class IHumansReceptors, Pattern RecognitionVirus DiseasesAntigens, CD1Histocompatibility Antigens Class IReceptors, Pattern Recognition

Identifiers

PMID19476512
PMCPMC2691781
OpenAlexW2091087670

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.