Evidence map›Paper›PMID 19124746›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Ig-like transcript 4 inhibits lipid antigen presentation through direct CD1d interaction.

Demin Li, Lili Wang, Li Yu, Eric C Freundt, Boquan Jin, Gavin R Screaton, Xiao-Ning Xu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
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  8. Single cell RNA-sequencing analysis reveals thatJHEP reports : innovation in hepatology · 2023
    Article
  9. Article
  10. Review
  11. Human γδ T cells recognize CD1b by two distinct mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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  14. Review
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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 at 4 institutions in 3 countries.

Demin LiMedical Research Council Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Headington, Oxford, UK. demin.li@imm.ox.ac.uk
Lili Wang
Li Yu
Eric C Freundt
Boquan Jin
Gavin R Screaton
Xiao-Ning Xu
John Radcliffe Hospital · GBNational Institutes of Health · USAir Force Medical University · CNHammersmith Hospital · GB

Funding

Molecular Pathways of Programmed Cell Death And Viral CytopathicityZIAAI000718 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SU, HELEN · 2009 to 2024
$4.5M
Molecular Pathways--Programmed Death/Viral CytopathicityZ01AI000718 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI LENARDO, MICHAEL · 1995 to 2008
$763k
Intramural NIH HHS Z01 AI000718Medical Research Council G0400720Medical Research Council G0600000Medical Research Council G0801508Medical Research Council MC_U137881015
6 · The paper itself

Abstract

NKT cells recognize lipid Ags presented by CD1d molecules and play an important role in the regulation of innate and adaptive immune responses. In this study, we report the identification of a membrane-associated protein, Ig-like transcript 4 (ILT4), as a novel human CD1d receptor that inhibits CD1d-mediated immune responses. We found that native CD1d tetramer generated by mammalian cells was able to specifically bind human monocytes in the peripheral blood, and this binding was at least partly mediated by monocyte-expressed ILT4. The interaction between ILT4 and CD1d involves the two N-terminal domains of ILT4 and the Ag-binding groove of CD1d (alpha1/alpha2 domain). This interaction has been identified on the cell surface as well as in the endosomal and lysosomal compartments. Functional analysis showed that ILT4 could block the loading of lipid Ags such as alpha-GalCer, and consequently inhibited NKT recognition. The interaction between ILT4 and CD1d may provide new insights into the regulation of NKT-mediated immunity.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsAntigens, CD1dCell LineCell MembraneCells, CulturedCytoplasmGalactosylceramidesHumansImmune ToleranceImmunity, CellularLymphocyte ActivationMembrane GlycoproteinsMonocytesProtein Bindingalpha-galactosylceramideAntigens, CD1dCD1D protein, humanGalactosylceramidesLILRB2 protein, humanMembrane GlycoproteinsReceptors, Immunologic

Identifiers

PMID19124746
PMCPMC2646168
OpenAlexW1914317420

What OpenQuestion holds

Textmetadata
LicenceTDM
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.