Evidence map›Paper›PMID 29320731›Full record

ArticleCell reports2018

Durable Interactions of T Cells with T Cell Receptor Stimuli in the Absence of a Stable Immunological Synapse.

Viveka Mayya, Edward Judokusumo, Enas Abu Shah, Christopher G Peel, Willie Neiswanger, David Depoil, David A Blair, Chris H Wiggins, Lance C Kam, Michael L Dustin

Abstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
  2. SLAMF7 (CD319) on activated CD8Cell death and differentiation · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Unraveling the mechanobiology of immune cells.Current opinion in biotechnology · 2020
    Review
  11. Regulatory T cells suppress Th17 cell CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Coreceptors and TCR Signaling - the Strong and the Weak of It.Frontiers in cell and developmental biology · 2020
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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.

Viveka MayyaKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK; Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Edward JudokusumoDepartment of Biological Engineering, Columbia University, New York, NY 10027, USA.
Enas Abu ShahKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK.
Christopher G PeelKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK.
Willie NeiswangerMachine Learning Department, Carnegie Mellon University, Pittsburgh, PA 15213, USA; Department of Applied Physics and Applied Mathematics, Columbia University, New York, NY 10027, USA.
David DepoilKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK.
David A BlairSkirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.
Chris H WigginsDepartment of Applied Physics and Applied Mathematics, Columbia University, New York, NY 10027, USA.
Lance C KamDepartment of Biological Engineering, Columbia University, New York, NY 10027, USA.
Michael L DustinKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK; Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA. Electronic address: michael.dustin@kennedy.ox.ac.uk.

Funding

Nanomedicine development center for mechanobiologyPN2EY016586 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2005 to 2014
$23.0M
Requirement for Sensitive T Cell Response to AntigenR37AI043542 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2007 to 2016
$3.6M
NEI NIH HHS PN2 EY016586NIAID NIH HHS R37 AI043542Wellcome TrustWellcome Trust 100262/Z/12/Z
6 · The paper itself

Abstract

T cells engage in two modes of interaction with antigen-presenting surfaces: stable synapses and motile kinapses. Although it is surmised that durable interactions of T cells with antigen-presenting cells involve synapses, in situ 3D imaging cannot resolve the mode of interaction. We have established in vitro 2D platforms and quantitative metrics to determine cell-intrinsic modes of interaction when T cells are faced with spatially continuous or restricted stimulation. All major resting human T cell subsets, except memory CD8 T cells, spend more time in the kinapse mode on continuous stimulatory surfaces. Surprisingly, we did not observe any concordant relationship between the mode and durability of interaction on cell-sized stimulatory spots. Naive CD8 T cells maintain kinapses for more than 3 hr before leaving stimulatory spots, whereas their memory counterparts maintain synapses for only an hour before leaving. Thus, durable interactions do not require stable synapses.

Indexed as

HumansImmunological SynapsesReceptors, Antigen, T-CellReceptors, Antigen, T-Celladhesionchemokinesimmunological synapsekinapselive imaginglymphocytesmicro-contact printingmigration

Identifiers

PMID29320731
PMCPMC5775504

What OpenQuestion holds

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Registered trials

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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.