Evidence map›Paper›PMID 15304644›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

The T cell antigen receptor expressed by Valpha14i NKT cells has a unique mode of glycosphingolipid antigen recognition.

Stéphane Sidobre, Kirsten J L Hammond, Lise Bénazet-Sidobre, Sergei D Maltsev, Stewart K Richardson, Rachel M Ndonye, Amy R Howell, Teruyuki Sakai, Gurdyal S Besra, Steven A Porcelli and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

45 citing papers in PubMed, 96 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Are fat NKT cells born that way?Cellular & molecular immunology · 2017
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Synthesis of a 2"-deoxy-β-GalCer.Molecules (Basel, Switzerland) · 2014
    Article
  14. Review
  15. Review
  16. T cells specific for lipid antigens.Immunologic research · 2012
    Review
  17. Review
  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

11 authors at 1 institution in 1 country.

Stéphane SidobreDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, CA 92121, USA.
Kirsten J L Hammond
Lise Bénazet-Sidobre
Sergei D Maltsev
Stewart K Richardson
Rachel M Ndonye
Amy R Howell
Teruyuki Sakai
Gurdyal S Besra
Steven A Porcelli
Mitchell Kronenberg
La Jolla Institute for Immunology · US

Funding

Precision Targeting of CD1-Restricted iNKT Cells for Cancer ImmunotherapyR01AI045889 · NIAID · YESHIVA UNIVERSITY · PI Steven A Porcelli · 1999 to 2026
$9.3M
Recognition of bacterial antigens by NKT cellsR01AI045053 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2000 to 2010
$3.3M
ANTIGEN PRESENTATION BY CD1CR01AI048933 · NIAID · YESHIVA UNIVERSITY · PI PORCELLI, STEVEN A · 2000 to 2004
$1.5M
PROTEIN-CARBOHYDRATE INTERACTIONS IN CELL COMMUNICATIONR24GM061502 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI PAULSON, JAMES C. · 2000 to 2000
$44k
NIAID NIH HHS R01 AI045053NIAID NIH HHS R01 AI045889NIAID NIH HHS R01 AI048933NIAID NIH HHS R01 AI45053NIAID NIH HHS R01 AI45889NIAID NIH HHS R01 AI48933NIGMS NIH HHS R24 GM061502NIGMS NIH HHS U54 GM61502
6 · The paper itself

Abstract

Natural killer (NK) T cells with an invariant Valpha14 rearrangement (Valpha14i) are the largest population of lipid antigen-specific T lymphocytes identified in animals. They react to the glycolipid alpha-galactosyl ceramide (alpha-GalCer) presented by CD1d, and they may have important regulatory functions. It was previously shown that the Valpha14i T cell antigen receptor (TCR) has a high affinity for the alpha-GalCer/CD1d complex, driven by a long half-life (t(1/2)). Although this result could have reflected the unique attributes of alpha-GalCer, using several related glycolipid compounds, we show here that the threshold for full activation of Valpha14i NKT cells by these glycosphingolipids requires a relatively high-affinity TCR interaction with a long t(1/2). Furthermore, our data are consistent with the view that the mechanism of recognition of these compounds presented by CD1d to the Valpha14i NKT cell TCR is likely to fit a lock-and-key model. Overall, these findings emphasize the distinct properties of glycosphingolipid antigen recognition by Valpha14i NKT cells.

Indexed as

AnimalsAntigensAntigens, CD1Antigens, CD1dBinding SitesCytokinesGlycosphingolipidsIn Vitro TechniquesKiller Cells, NaturalKineticsMacromolecular SubstancesMiceMice, Inbred C57BLReceptors, Antigen, T-CellSolubilityT-Lymphocyte SubsetsAntigensAntigens, CD1Antigens, CD1dCytokinesGlycosphingolipidsMacromolecular SubstancesReceptors, Antigen, T-Cell

Identifiers

PMID15304644
PMCPMC514465
OpenAlexW1971066229

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.