Evidence map›Paper›PMID 12511872›Full record

ReviewNature reviews. Immunology2003

Intracellular pathways of CD1 antigen presentation.

D Branch Moody, Steven A Porcelli

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Immunology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 193 citations in OpenAlex.

  1. Trial
  2. Article
  3. CD1a and Lipids as Mediators of T Cell Activation in the Skin.The Journal of investigative dermatology · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Insights into the CD1 lipidome.Frontiers in immunology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. MR1: An unconventional twist in the tail.The Journal of cell biology · 2022
    Article
  13. Article
  14. Article
  15. A humanized mouse model forFrontiers in immunology · 2022
    Article
  16. Article
  17. CD1a function in human skin disease.Molecular immunology · 2021
    Review
  18. Article
  19. Article
  20. Article

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

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

2 authors at 2 institutions in 1 country.

D Branch MoodyDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, 1 Jimmy Fund Way, Boston, Massachusetts 02114, USA. bmoody@rics.bwh.harvard.edu
Steven A Porcelli
Albert Einstein College of Medicine · USBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Each of the human CD1 proteins takes a different route through secretory and endocytic compartments before finally arriving at the cell surface, where these proteins present glycolipid antigens to T cells. Recent studies have shown that adaptor-protein complexes and CD1-associated chaperones control not only CD1 trafficking, but also the development and activation of CD1-restricted T cells. This indicates that CD1 proteins, similar to MHC class I and II molecules, selectively acquire certain antigens in distinct cellular subcompartments. Here, we summarize evidence supporting the hypothesis that CD1 proteins use separate, but parallel, pathways to survey endosomal compartments differentially for lipid antigens.

Indexed as

Adaptor Proteins, Vesicular TransportAmino Acid SequenceAnimalsAntigen PresentationAntigen-Presenting CellsAntigens, CD1EndosomesHumansMolecular Sequence DataProtein IsoformsAdaptor Proteins, Vesicular TransportAntigens, CD1Protein Isoforms

Identifiers

PMID12511872
OpenAlexW1966344619

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.