Evidence map›Paper›PMID 25283967›Full record

ReviewTrends in immunology2014

γδ T cell surveillance via CD1 molecules.

Adrienne M Luoma, Caitlin D Castro, Erin J Adams

Abstract readReview
In one paragraph

Review in Trends in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–field-weighted citation impact
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

53 citing papers in PubMed.

  1. Review
  2. Article
  3. Detergents alter the stability and lipid binding properties of the CD1d immunoreceptor.Protein science : a publication of the Protein Society · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Revisiting T Cells in Chronic Rhinosinusitis.Allergy, asthma & immunology research · 2024
    Review
  8. Function of unconventional T cells in oral lichen planus revealed by single-cell RNA sequencing.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  9. Cytomegalovirus drives Vδ1Nature communications · 2024
    Article
  10. Review
  11. The therapeutic role of γδT cells in TNBC.Frontiers in immunology · 2024
    Review
  12. Review
  13. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  14. Article
  15. Review
  16. Review
  17. T cells in health and disease.Signal transduction and targeted therapy · 2023
    Review
  18. Review
  19. Review
  20. Innate immunity and early liver inflammation.Frontiers in immunology · 2023
    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.

Adrienne M LuomaCommittee on Immunology and Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Caitlin D CastroCommittee on Immunology and Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Erin J AdamsCommittee on Immunology and Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA. Electronic address: ejadams@uchicago.edu.

Funding

Molecular Recognition of Ligand by the Gamma Delta T Cell ReceptorR01AI073922 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2007 to 2016
$3.8M
Molecular studies of lipid presentation and T cell recognition of CD1cR56AI097386 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2013 to 2013
$366k
NIAID NIH HHS R01 AI073922NIAID NIH HHS R56 AI097386
6 · The paper itself

Abstract

γδ T cells are a prominent epithelial-resident lymphocyte population, possessing multi-functional capacities in the repair of host tissue, pathogen clearance, and tumor surveillance. Although three decades have now passed since their discovery, the nature of γδ T cell receptor (TCR)-mediated ligand recognition remains poorly defined. Recent studies have provided structural insight into this recognition, demonstrating that γδ T cells survey both CD1 and the presented lipid, and in some cases are exquisitely lipid specific. We review these findings here, examining the molecular basis for and the functional relevance of this interaction. We discuss potential implications on the notion that non-classical major histocompatibility complex (MHC) molecules may function as important restricting elements of γδ TCR specificity, and on our understanding of γδ T cell activation and function.

Indexed as

CD1dcrystallographylipidsrestrictionT cell receptorγδT cells

Identifiers

PMID25283967
PMCPMC4383740

What OpenQuestion holds

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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.