Evidence map›Paper›PMID 24239091›Full record

ArticleImmunity2013

Crystal structure of Vδ1 T cell receptor in complex with CD1d-sulfatide shows MHC-like recognition of a self-lipid by human γδ T cells.

Adrienne M Luoma, Caitlin D Castro, Toufic Mayassi, Leslie A Bembinster, Li Bai, Damien Picard, Brian Anderson, Louise Scharf, Jennifer E Kung, Leah V Sibener and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers.

0numbers the graph read from it
0cells of the map it votes in
179citing papers in PubMed
9.5field-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

179 citing papers in PubMed, 241 citations in OpenAlex.

  1. Trial
  2. γδ T cells in colorectal and liver cancer.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Harnessing Vδ1Frontiers in immunology · 2026
    Review
  10. Detergents alter the stability and lipid binding properties of the CD1d immunoreceptor.Protein science : a publication of the Protein Society · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

119 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Adrienne M LuomaCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA; Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Caitlin D CastroDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Toufic MayassiCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA; Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Leslie A BembinsterDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Li BaiInstitute of Immunology, School of Life Sciences, University of Science and Technology of China, Hefei 230027, China; Department of Pathology, University of Chicago, Chicago, IL 60637, USA; Howard Hughes Medical Institute.
Damien PicardDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA; Howard Hughes Medical Institute.
Brian AndersonDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA.
Louise ScharfDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Jennifer E KungDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Leah V SibenerDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.
Paul B SavageDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA.
Bana JabriCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA; Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Albert BendelacCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA; Department of Pathology, University of Chicago, Chicago, IL 60637, USA; Howard Hughes Medical Institute.
Erin J AdamsCommittee on Immunology, University of Chicago, Chicago, IL 60637, USA; Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA. Electronic address: ejadams@uchicago.edu.
University of Chicago · USBrigham Young University · USHoward Hughes Medical Institute · USUniversity of Science and Technology of China · CN

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI LIU, CAMBRIAN YANGSHAO · 1990 to 2025
$29.8M
Th1/Th2 Glycolipid AdjuvantsP01AI053725 · NIAID · UNIVERSITY OF CHICAGO · PI TEYTON, LUC · 2003 to 2012
$11.8M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Innate and adaptive immunity in celiac diseaseR01DK067180 · NIDDK · UNIVERSITY OF CHICAGO · PI JABRI, BANA · 2005 to 2024
$8.5M
Transcriptional Regulation of Innate-Like T CellsR01AI038339 · NIAID · UNIVERSITY OF CHICAGO · PI ESTERHAZY, DARIA · 1996 to 2025
$7.6M
Molecular Recognition of Ligand by the Gamma Delta T Cell ReceptorR01AI073922 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2007 to 2016
$3.8M
Molecular studies of lipid presentation and T cell recognition of CD1cR56AI097386 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2013 to 2013
$366k
Howard Hughes Medical InstituteNIAID NIH HHS P01 AI053725NIAID NIH HHS R01 AI038339NIAID NIH HHS R01 AI073922NIAID NIH HHS R01_AI073922NIAID NIH HHS R56 AI097386NIAID NIH HHS R56_AI097386NIAID NIH HHS T32 AI007090NIDDK NIH HHS P30_DK42086NIDDK NIH HHS R01 DK067180NIDDK NIH HHS R01_DK67180
6 · The paper itself

Abstract

The nature of the antigens recognized by γδ T cells and their potential recognition of major histocompatibility complex (MHC)-like molecules has remained unclear. Members of the CD1 family of lipid-presenting molecules are suggested ligands for Vδ1 TCR-expressing γδ T cells, the major γδ lymphocyte population in epithelial tissues. We crystallized a Vδ1 TCR in complex with CD1d and the self-lipid sulfatide, revealing the unusual recognition of CD1d by germline Vδ1 residues spanning all complementarity-determining region (CDR) loops, as well as sulfatide recognition separately encoded by nongermline CDR3δ residues. Binding and functional analysis showed that CD1d presenting self-lipids, including sulfatide, was widely recognized by gut Vδ1+ γδ T cells. These findings provide structural demonstration of MHC-like recognition of a self-lipid by γδ T cells and reveal the prevalence of lipid recognition by innate-like T cell populations.

Indexed as

Models, MolecularAnimalsAntigen PresentationAntigens, CD1dCrystallography, X-RayEpitopesHumansJurkat CellsLipidsMajor Histocompatibility ComplexProtein Structure, QuaternaryReceptors, Antigen, T-Cell, gamma-deltaSulfoglycosphingolipidsT-LymphocytesAntigens, CD1dEpitopesLipidsReceptors, Antigen, T-Cell, gamma-deltaSulfoglycosphingolipids

Identifiers

PMID24239091
PMCPMC3875342
OpenAlexW2040154148

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.