Evidence map›Paper›PMID 12682111›Full record

ArticleThe Journal of experimental medicine2003

Ligand-dependent inhibition of CD1d-restricted NKT cell development in mice transgenic for the activating receptor Ly49D.

Roger B Voyle, Friedrich Beermann, Rosemary K Lees, Jens Schümann, Jacques Zimmer, Werner Held, H Robson MacDonald

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. The α glycolipid rules the NKT cell TCR.The Journal of experimental medicine · 2025
    Article
  2. NKT Cells Contribute to the Control of Microbial Infections.Frontiers in cellular and infection microbiology · 2021
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Diverse cytokine production by NKT cell subsets and identification of an IL-17-producing CD4-NK1.1- NKT cell population.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. 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

7 authors.

Roger B VoyleLudwig Institute for Cancer Research, Chemin des Boveresses 155, CH-1066 Epalinges, Switzerland. hughrobson.macdonald@isrec.unil.ch
Friedrich Beermann
Rosemary K Lees
Jens Schümann
Jacques Zimmer
Werner Held
H Robson MacDonald

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to their CD1d-restricted T cell receptor (TCR), natural killer T (NKT) cells express various receptors normally associated with NK cells thought to act, in part, as modulators of TCR signaling. Immunoreceptor-tyrosine activation (ITAM) and inhibition (ITIM) motifs associated with NK receptors may augment or attenuate perceived TCR signals respectively, potentially influencing NKT cell development and function. ITIM-containing Ly49 family receptors expressed by NKT cells are proposed to play a role in their development and function. We have produced mice transgenic for the ITAM-associated Ly49D and ITIM-containing Ly49A receptors and their common ligand H2-Dd to determine the importance of these signaling interplays in NKT cell development. Ly49D/H2-Dd transgenic mice had selectively and severely reduced numbers of thymic and peripheral NKT cells, whereas both ligand and Ly49D transgenics had normal numbers of NKT cells. CD1d tetramer staining revealed a blockade of NKT cell development at an early precursor stage. Coexpression of a Ly49A transgene partially rescued NKT cell development in Ly49D/H2-Dd transgenics, presumably due to attenuation of ITAM signaling. Thus, Ly49D-induced ITAM signaling is incompatible with the early development of cells expressing semi-invariant CD1d-restricted TCRs and appropriately harmonized ITIM-ITAM signaling is likely to play an important role in the developmental program of NKT cells.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid MotifsAnimalsAntigens, CD1Antigens, CD1dAntigens, LyH-2 AntigensHistocompatibility Antigen H-2DKiller Cells, NaturalLectins, C-TypeLigandsMembrane ProteinsMiceMice, Inbred C57BLMice, Inbred DBAMice, TransgenicAdaptor Proteins, Signal TransducingAntigens, CD1Antigens, CD1dAntigens, LyH-2 AntigensHistocompatibility Antigen H-2DKlra1 protein, mouseKlra4 protein, mouseLectins, C-TypeLigandsMembrane ProteinsNK Cell Lectin-Like Receptor Subfamily AReceptors, Antigen, T-Cell, alpha-betaReceptors, ImmunologicReceptors, NK Cell Lectin-LikeTYROBP protein, human

Identifiers

PMID12682111
PMCPMC2193884

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.