Evidence map›Paper›PMID 21666690›Full record

ArticleNature immunology2011

A semi-invariant Vα10+ T cell antigen receptor defines a population of natural killer T cells with distinct glycolipid antigen-recognition properties.

Adam P Uldrich, Onisha Patel, Garth Cameron, Daniel G Pellicci, E Bridie Day, Lucy C Sullivan, Konstantinos Kyparissoudis, Lars Kjer-Nielsen, Julian P Vivian, Benjamin Cao and 10 more

Abstract read
In one paragraph

Article in Nature immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
  2. Article
  3. Lipidomic scanning of self-lipids identifies headless antigens for natural killer T cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
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  8. Review
  9. Benzofuran sulfonates and small self-lipid antigens activate type II NKT cells via CD1d.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. NKT Cells Contribute to the Control of Microbial Infections.Frontiers in cellular and infection microbiology · 2021
    Review
  11. Review
  12. Article
  13. Article
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  15. Article
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12 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

20 authors at 4 institutions in 3 countries.

Adam P UldrichDepartment of Microbiology and Immunology, The University of Melbourne, Parkville, Victoria, Australia.
Onisha Patel
Garth Cameron
Daniel G Pellicci
E Bridie Day
Lucy C Sullivan
Konstantinos Kyparissoudis
Lars Kjer-Nielsen
Julian P Vivian
Benjamin Cao
Andrew G Brooks
Spencer J Williams
Petr Illarionov
Gurdyal S Besra
Stephen J Turner
Steven A Porcelli
James McCluskey
Mark J Smyth
Jamie Rossjohn
Dale I Godfrey
University of Melbourne · AUMonash University · AUUniversity of Birmingham · GBAlbert Einstein College of Medicine · US

Funding

Precision Targeting of CD1-Restricted iNKT Cells for Cancer ImmunotherapyR01AI045889 · NIAID · YESHIVA UNIVERSITY · PI Steven A Porcelli · 1999 to 2026
$9.3M
NIAID NIH HHS AI45889NIAID NIH HHS R01 AI045889
6 · The paper itself

Abstract

Type I natural killer T cells (NKT cells) are characterized by an invariant variable region 14-joining region 18 (V(α)14-J(α)18) T cell antigen receptor (TCR) α-chain and recognition of the glycolipid α-galactosylceramide (α-GalCer) restricted to the antigen-presenting molecule CD1d. Here we describe a population of α-GalCer-reactive NKT cells that expressed a canonical V(α)10-J(α)50 TCR α-chain, which showed a preference for α-glucosylceramide (α-GlcCer) and bacterial α-glucuronic acid-containing glycolipid antigens. Structurally, despite very limited TCRα sequence identity, the V(α)10 TCR-CD1d-α-GlcCer complex had a docking mode similar to that of type I TCR-CD1d-α-GalCer complexes, although differences at the antigen-binding interface accounted for the altered antigen specificity. Our findings provide new insight into the structural basis and evolution of glycolipid antigen recognition and have notable implications for the scope and immunological role of glycolipid-specific T cell responses.

Indexed as

Adjuvants, ImmunologicAmino Acid SequenceAnimalsAntigens, BacterialAntigens, CD1dCell LineGalactosylceramidesGlucuronatesHumansMiceMice, Mutant StrainsMolecular Sequence DataNatural Killer T-CellsReceptors, Antigen, T-Cell, alpha-betaAdjuvants, Immunologicalpha-galactosylceramideAntigens, BacterialAntigens, CD1dGalactosylceramidesGlucuronatesKRN 7000Receptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID21666690
PMCPMC5584938
OpenAlexW2094446788

What OpenQuestion holds

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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.