Evidence map›Paper›PMID 19968559›Full record

ReviewAnnual review of immunology2010

Functional anatomy of T cell activation and synapse formation.

David R Fooksman, Santosh Vardhana, Gaia Vasiliver-Shamis, Jan Liese, David A Blair, Janelle Waite, Catarina Sacristán, Gabriel D Victora, Alexandra Zanin-Zhorov, Michael L Dustin

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 267 papers.

0numbers the graph read from it
0cells of the map it votes in
267citing papers in PubMed
13.0field-weighted citation impact, top 1% 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

267 citing papers in PubMed, 441 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. SLAMF7 (CD319) on activated CD8Cell death and differentiation · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Mathematical models of TCR initial triggering.Frontiers in immunology · 2024
    Review
  15. Article
  16. Multifaceted control of T cell differentiation by STIM1.Trends in biochemical sciences · 2023
    Review
  17. Integrin α3 promotes TScience immunology · 2023
    Article
  18. Article
  19. Article
  20. Article

207 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 1 institution in 1 country.

David R FooksmanDepartment of Molecular Pathogenesis, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, 10016, USA. David.Fooksman@med.nyu.edu
Santosh Vardhana
Gaia Vasiliver-Shamis
Jan Liese
David A Blair
Janelle Waite
Catarina Sacristán
Gabriel D Victora
Alexandra Zanin-Zhorov
Michael L Dustin
New York University · US

Funding

Nanomedicine development center for mechanobiologyPN2EY016586 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2005 to 2014
$23.0M
Visualizing, Quantifying, and Modeling of T Cell Response to Listeria InfectionP01AI071195 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CHAKRABORTY, ARUP K. · 2006 to 2010
$8.1M
Requirement for Sensitive T Cell Response to AntigenR37AI043542 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2007 to 2016
$3.6M
Environmental Control of the Immunological SynapseR01AI055037 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2004 to 2014
$3.6M
PHYSIOLOGICAL CHEMISTRY OF INTEGRIN FUNCTIONR01AI044931 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 1999 to 2007
$1.5M
Physiological Chemistry of Integrin FunctionR56AI044931 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2009 to 2010
$474k
Environmental Control of the Immunological SynapseR21AI055037 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL L · 2003 to 2003
$405k
NEI NIH HHS PN2 EY016586NIAID NIH HHS P01 AI071195NIAID NIH HHS R01 AI055037NIAID NIH HHS R37 AI043542NIAID NIH HHS R56 AI044931
6 · The paper itself

Abstract

T cell activation and function require a structured engagement of antigen-presenting cells. These cell contacts are characterized by two distinct dynamics in vivo: transient contacts resulting from promigratory junctions called immunological kinapses or prolonged contacts from stable junctions called immunological synapses. Kinapses operate in the steady state to allow referencing to self-peptide-MHC (pMHC) and searching for pathogen-derived pMHC. Synapses are induced by T cell receptor (TCR) interactions with agonist pMHC under specific conditions and correlate with robust immune responses that generate effector and memory T cells. High-resolution imaging has revealed that the synapse is highly coordinated, integrating cell adhesion, TCR recognition of pMHC complexes, and an array of activating and inhibitory ligands to promote or prevent T cell signaling. In this review, we examine the molecular components, geometry, and timing underlying kinapses and synapses. We integrate recent molecular and physiological data to provide a synthesis and suggest ways forward.

Indexed as

Lymphocyte ActivationAnimalsCell CommunicationHumansImmunological SynapsesReceptors, Antigen, T-CellSignal TransductionT-LymphocytesReceptors, Antigen, T-Cell

Identifiers

PMID19968559
PMCPMC2885351
OpenAlexW2127424425

What OpenQuestion holds

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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.