Evidence map›Paper›PMID 31469364›Full record

ArticleeLife2019

Composition and structure of synaptic ectosomes exporting antigen receptor linked to functional CD40 ligand from helper T cells.

David G Saliba, Pablo F Céspedes-Donoso, Štefan Bálint, Ewoud B Compeer, Kseniya Korobchevskaya, Salvatore Valvo, Viveka Mayya, Audun Kvalvaag, Yanchun Peng, Tao Dong and 6 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

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  12. Proceedings of the National Academy of Sciences of the United States of America · 2025
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  18. The physical landscape of CAR-T synapse.Biophysical journal · 2024
    Review
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4 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

16 authors at 3 institutions in 2 countries.

David G Saliba *Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-9523-0586
Pablo F Céspedes-Donoso *Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-1641-4107
Štefan Bálint *Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-4470-5881
Ewoud B CompeerKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-3050-7633
Kseniya KorobchevskayaKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.
Salvatore ValvoKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.
Viveka MayyaKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.
Audun KvalvaagKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.
Yanchun PengMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Tao DongMRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-3545-3758
Maria-Laura TognoliDepartment of Oncology, University of Oxford, Oxford, United Kingdom.
Eric O'NeillDepartment of Oncology, University of Oxford, Oxford, United Kingdom.
Sarah BonhamDiscovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Roman FischerDiscovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9715-5951
Benedikt M KesslerDiscovery Proteomics Facility, Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Michael L DustinKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-4983-6389
Nuffield Orthopaedic Centre · GBUniversity of Oxford · GBUniversity of Malta · MT

Funding

Requirement for Sensitive T Cell Response to AntigenR37AI043542 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2007 to 2016
$3.6M
REQUIREMENT FOR SENSITIVE T CELL RESPONSE TO ANTIGENR01AI043542 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL L · 1999 to 2005
$1.5M
Cancer Research UK UK A19277Chinese Academy of Sciences 2018-I2M-2-002European Commission AdG 670930European Molecular Biology Organization ALTF 1420-2015European Molecular Biology Organization ALTF 1420-2015 (in conjunction with the European Commission (LTFCOFUND2013, GA-2013-609409) and Marie Sklodowska-Curie Actions).H2020 Marie Skłodowska-Curie Actions The Research Council of Norway in conjunction with Marie Sklodowska-Curie Actions 275466Kennedy Trust for Rheumatology Research N/AMedical Research Council G0600520Medical Research Council G1001046NIAID NIH HHS R01 AI043542NIAID NIH HHS R37 AI043542NIH HHS AI043542NIH HHS N/AResearch Council of Norway The Research Council of Norway in conjunction with Marie Sklodowska-Curie Actions 275466The Research Council of Norway in conjunction with Marie Sklodowska-Curie Actions 275466Wellcome PRF 100262Wellcome Trust
6 · The paper itself

Abstract

Planar supported lipid bilayers (PSLB) presenting T cell receptor (TCR) ligands and ICAM-1 induce budding of extracellular microvesicles enriched in functional TCR, defined here as synaptic ectosomes (SE), from helper T cells. SE bind peptide-MHC directly exporting TCR into the synaptic cleft, but incorporation of other effectors is unknown. Here, we utilized bead supported lipid bilayers (BSLB) to capture SE from single immunological synapses (IS), determined SE composition by immunofluorescence flow cytometry and enriched SE for proteomic analysis by particle sorting. We demonstrate selective enrichment of CD40L and ICOS in SE in response to addition of CD40 and ICOSL, respectively, to SLB presenting TCR ligands and ICAM-1. SE are enriched in tetraspanins, BST-2, TCR signaling and ESCRT proteins. Super-resolution microscopy demonstrated that CD40L is present in microclusters within CD81 defined SE that are spatially segregated from TCR/ICOS/BST-2. CD40L

Indexed as

CD40 LigandCell-Derived MicroparticlesCytokinesDendritic CellsFlow CytometryFluorescent Antibody TechniqueHumansProteomeReceptors, AntigenT-Lymphocytes, Helper-InducerCD40 LigandCytokinesProteomeReceptors, AntigenCD40LCRISPR/Cas9extracellular vesicleshumanICOSimmune synapseimmunologyinflammationtetraspanins

Identifiers

PMID31469364
PMCPMC6748831
OpenAlexW2970588659

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.