Evidence map›Paper›PMID 25197085›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Activation of iNKT cells by a distinct constituent of the endogenous glucosylceramide fraction.

Patrick J Brennan, Raju V V Tatituri, Christian Heiss, Gerald F M Watts, Fong-Fu Hsu, Natacha Veerapen, Liam R Cox, Parastoo Azadi, Gurdyal S Besra, Michael B Brenner

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Frontiers in immunology · 2023
    Review
  3. Innate and Innate-like Effector Lymphocytes in Health and Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. NKT Cells Contribute to the Control of Microbial Infections.Frontiers in cellular and infection microbiology · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Innate T cells in the intensive care unit.Molecular immunology · 2019
    Review
  17. Article
  18. Innate T Cells Govern Adipose Tissue Biology.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  19. Review
  20. Article

5 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

10 authors at 5 institutions in 2 countries.

Patrick J BrennanDepartment of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Raju V V TatituriDepartment of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Christian HeissComplex Carbohydrate Research Center, University of Georgia, Athens, GA 30602;
Gerald F M WattsDepartment of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Fong-Fu HsuDivision of Endocrinology, Metabolism and Lipid Research, Washington University, St. Louis, MO 63110;
Natacha VeerapenSchool of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom; and.
Liam R CoxSchool of Chemistry, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Parastoo AzadiComplex Carbohydrate Research Center, University of Georgia, Athens, GA 30602;
Gurdyal S BesraSchool of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom; and.
Michael B BrennerDepartment of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; mbrenner@partners.org.
Harvard University · USUniversity of Birmingham · GBUniversity of Georgia · USBrigham and Women's Hospital · USWashington University in St. Louis · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Kristin A Knouse · 1985 to 2026
$93.9M
Transgenic CoreP30DK057521 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KAHN, BARBARA B. · 2000 to 2019
$31.4M
Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2012 to 2019
$12.0M
CD1d-restricted T Cell Self-antigens and InfectionR01AI063428 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B. · 2005 to 2015
$3.9M
Regulatory iNKT Cells Suppress Inflammation and Drive ThermogenesisR01AI113046 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B. · 2014 to 2023
$3.9M
Self and dietary lipid antigens for invariant natural killer T cellsK08AI102945 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNAN, PATRICK JOSEPH · 2013 to 2016
$736k
CD1d and NKT Cell Activation and Function in InfectionR56AI063428 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B. · 2010 to 2010
$433k
Medical Research Council G1001750NCI NIH HHS P30-CA14051NIAID NIH HHS AI063428NIAID NIH HHS AI1007306NIAID NIH HHS AI1028973NIAID NIH HHS AI102945NIAID NIH HHS HHSN272201300006CNIAID NIH HHS K08 AI102945NIAID NIH HHS R01 AI063428NIAID NIH HHS R01 AI113046NIAID NIH HHS R56 AI063428NIDDK NIH HHS DK057521NIDDK NIH HHS DK20579NIDDK NIH HHS DK56341NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK056341NIDDK NIH HHS P30 DK057521NIDDK NIH HHS P60 DK020579NIGMS NIH HHS GM103422NIGMS NIH HHS P41 GM103422
6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells are a specialized T-cell subset that recognizes lipids as antigens, contributing to immune responses in diverse disease processes. Experimental data suggests that iNKT cells can recognize both microbial and endogenous lipid antigens. Several candidate endogenous lipid antigens have been proposed, although the contextual role of specific antigens during immune responses remains largely unknown. We have previously reported that mammalian glucosylceramides (GlcCers) activate iNKT cells. GlcCers are found in most mammalian tissues, and exist in variable molecular forms that differ mainly in N-acyl fatty acid chain use. In this report, we purified, characterized, and tested the GlcCer fractions from multiple animal species. Although activity was broadly identified in these GlcCer fractions from mammalian sources, we also found activity properties that could not be reconciled by differences in fatty acid chain use. Enzymatic digestion of β-GlcCer and a chromatographic separation method demonstrated that the activity in the GlcCer fraction was limited to a rare component of this fraction, and was not contained within the bulk of β-GlcCer molecular species. Our data suggest that a minor lipid species that copurifies with β-GlcCer in mammals functions as a lipid self antigen for iNKT cells.

Indexed as

AnimalsCattleChromatography, Thin LayerGlucosylceramidaseGlucosylceramidesHumansLymphocyte ActivationMass SpectrometryMiceMilkNatural Killer T-CellsGlucosylceramidaseGlucosylceramidesanomerantigen presentationCD1ddietary antigenself-reactive

Identifiers

PMID25197085
PMCPMC4169973
OpenAlexW2024436717

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.