Evidence map›Paper›PMID 26755823›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Molecular Analysis of Lipid-Reactive Vδ1 γδ T Cells Identified by CD1c Tetramers.

Sobhan Roy, Dalam Ly, Caitlin D Castro, Nan-Sheng Li, Andrew J Hawk, John D Altman, Stephen C Meredith, Joseph A Piccirilli, D Branch Moody, Erin J Adams

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

66 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Functions of Sulfatide in the Nervous, Immune, and Urinary Systems.Advances in experimental medicine and biology · 2026
    Review
  5. Harnessing Vδ1Frontiers in immunology · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. A GD (Gamma-Delta) type of cancel culture.Immuno-oncology technology · 2024
    Review
  12. Cancer immunotherapy by γδ T cells.Science (New York, N.Y.) · 2024
    Review
  13. Article
  14. The Evolving Portrait of γδ TCR Recognition Determinants.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  20. Review

6 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 3 institutions in 2 countries.

Sobhan RoyDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637;ORCID http://orcid.org/0000-0003-3511-7869
Dalam LyDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA 02115; Department of Immunology, University of Toronto, Toronto, Ontario M5S 1A8, Canada;ORCID http://orcid.org/0000-0002-1177-0225
Caitlin D CastroDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; Committee on Immunology, University of Chicago, Chicago, IL 60637;
Nan-Sheng LiDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637;
Andrew J HawkDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; Department of Pathology, University of Chicago, Chicago, IL 60637;
John D AltmanDepartment of Microbiology and Immunology, Emory Vaccine Center at Yerkes, Emory University School of Medicine, Atlanta, GA 30329; and.
Stephen C MeredithDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; Department of Pathology, University of Chicago, Chicago, IL 60637;
Joseph A PiccirilliDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; Department of Chemistry, University of Chicago, Chicago, IL 60637.
D Branch MoodyDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA 02115; ejadams@uchicago.edu bmoody@partners.org.ORCID http://orcid.org/0000-0003-2306-3058
Erin J AdamsDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; Committee on Immunology, University of Chicago, Chicago, IL 60637; ejadams@uchicago.edu bmoody@partners.org.
University of Chicago · USBrigham and Women's Hospital · USEmory University · US

Funding

Metabolomics Core U19AI111224 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI MOODY, DAVID BRANCH, MURRAY, MEGAN B · 2015 to 2021
$20.4M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
RESEARCH TRAINING IN RESPIRATORY BIOLOGYT32HL007605 · NHLBI · UNIVERSITY OF CHICAGO · PI Yun Fang, Gokhan M. Mutlu · 1985 to 2026
$18.1M
T cell response to CDI-restricted lipids in tuberculosisR01AI049313 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI MOODY, DAVID BRANCH · 2001 to 2025
$10.6M
CD1 Presentation of Self Lipids to Human T CellsR01AR048632 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI MOODY, DAVID BRANCH · 2002 to 2024
$9.4M
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
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS T32 HL007605NIAID NIH HHS R01 AI049313NIAID NIH HHS R01 AI073922NIAID NIH HHS R56 AI097386NIAID NIH HHS U19 AI111224NIAMS NIH HHS R01 AR048632
6 · The paper itself

Abstract

CD1c is abundantly expressed on human dendritic cells (DC) and B cells, where it binds and displays lipid Ags to T cells. In this study, we report that CD1c tetramers carrying Mycobacterium tuberculosis phosphomycoketide bind γδ TCRs. An unbiased method of ligand-based TCR selection detects interactions only with Vδ1(+) TCRs, and mutational analyses demonstrate a role of the Vδ1 domain during recognition. These results strengthen evidence for a role of CD1c in the γδ T cell response, providing biophysical evidence for CD1c-γδ TCR interactions and a named foreign Ag. Surprisingly, TCRs also bind CD1c complexes formed with diverse lipids such as lysophosphatidylcholine, sulfatide, or mannosyl-phosophomycoketide, but not lipopeptide ligands. Dissection of TCR interactions with CD1c carrying foreign Ags, permissive ligands, and nonpermissive lipid ligands clarifies the molecular basis of the frequently observed but poorly understood phenomenon of mixed self- and foreign Ag reactivity in the CD1 system.

Indexed as

Antigen PresentationAntigens, CD1Flow CytometryGlycoproteinsHumansLigandsLymphocyte ActivationPolymerase Chain ReactionReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsTransduction, GeneticAntigens, CD1CD1C protein, humanGlycoproteinsLigandsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID26755823
PMCPMC4744554
OpenAlexW2238814703

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.