Evidence map›Paper›PMID 29460282›Full record

ReviewImmunology2018

The versatility of the CD1 lipid antigen presentation pathway.

Andrew Chancellor, Stephan D Gadola, Salah Mansour

Open access · bronzeAbstract readReview
In one paragraph

Review in Immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Article
  3. Metabolites · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. A guide to antigen processing and presentation.Nature reviews. Immunology · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Andrew ChancellorFaculty of Medicine, Academic Unit of Clinical and Experimental Sciences, Southampton, UK.
Stephan D GadolaFaculty of Medicine, Academic Unit of Clinical and Experimental Sciences, Southampton, UK.
Salah MansourFaculty of Medicine, Academic Unit of Clinical and Experimental Sciences, Southampton, UK.ORCID 0000-0002-5982-734X
Roche (Switzerland) · CH

Funding

Cancer Research UK 23562
6 · The paper itself

Abstract

The family of non-classical major histocompatibility complex (MHC) class-I like CD1 molecules has an emerging role in human disease. Group 1 CD1 includes CD1a, CD1b and CD1c, which function to display lipids on the cell surface of antigen-presenting cells for direct recognition by T-cells. The recent advent of CD1 tetramers and the identification of novel lipid ligands has contributed towards the increasing number of CD1-restricted T-cell clones captured. These advances have helped to identify novel donor unrestricted and semi-invariant T-cell populations in humans and new mechanisms of T-cell recognition. However, although there is an opportunity to design broadly acting lipids and harness the therapeutic potential of conserved T-cells, knowledge of their role in health and disease is lacking. We briefly summarize the current evidence implicating group 1 CD1 molecules in infection, cancer and autoimmunity and show that although CD1 are not as diverse as MHC, recent discoveries highlight their versatility as they exhibit intricate mechanisms of antigen presentation.

Indexed as

Signal TransductionAnimalsAntigen PresentationAntigens, CD1AutoimmunityDisease SusceptibilityHumansHydrophobic and Hydrophilic InteractionsLigandsLipidsStructure-Activity RelationshipT-LymphocytesAntigens, CD1LigandsLipidsCD1cholesteryl-esterslipidsMycobacterium tuberculosismycolic acidT-cells

Identifiers

PMID29460282
PMCPMC5980215
OpenAlexW2793564129

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.