Evidence map›Paper›PMID 22547816›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Cytotoxic immunological synapses do not restrict the action of interferon-γ to antigenic target cells.

Nicholas Stephen Rennie Sanderson, Mariana Puntel, Kurt M Kroeger, Niyati S Bondale, Mark Swerdlow, Niloufar Iranmanesh, Hideo Yagita, Ahmed Ibrahim, Maria G Castro, Pedro R Lowenstein

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Defining lytic IFNγ for deciphering the CTL mechanism.Cellular & molecular immunology · 2026
    Article
  2. Article
  3. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. The spread of interferon-γ in melanomas is highly spatially confined, driving nongenetic variability in tumor cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Cytotoxic CD4Frontiers in immunology · 2023
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Modulation of the tumor micro-environment by CD8Current opinion in immunology · 2021
    Review
  17. Article
  18. Observational
  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.

Nicholas Stephen Rennie SandersonDepartment of Neurosurgery, The University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Mariana Puntel
Kurt M Kroeger
Niyati S Bondale
Mark Swerdlow
Niloufar Iranmanesh
Hideo Yagita
Ahmed Ibrahim
Maria G Castro
Pedro R Lowenstein

Funding

Gutless Adenovirus Mediated Gene Therapy for GliomaU01NS052465 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CASTRO, MARIA G · 2007 to 2011
$3.1M
Engineering the Brain Immune System for Tumor TherapyR01NS057711 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CASTRO, MARIA G · 2009 to 2013
$2.0M
Gene Therapy for Neurological DiseasesR01NS042893 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI LOWENSTEIN, PEDRO R · 2002 to 2006
$1.8M
Brain immune responses:Cellular & Molecular MechanismsR01NS061107 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOWENSTEIN, PEDRO R. · 2008 to 2012
$1.7M
Gene Therapy and the Brain: Neuroimmune InteractionsR01NS054193 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOWENSTEIN, PEDRO R. · 2007 to 2011
$1.6M
NINDS NIH HHS 1 R01 NS 054193NINDS NIH HHS 1R01-NS 057711NINDS NIH HHS 1U01 NS052465.01NINDS NIH HHS R01 NS042893NINDS NIH HHS R01 NS054193NINDS NIH HHS R01 NS057711NINDS NIH HHS R01 NS061107NINDS NIH HHS R01 NS 42893NINDS NIH HHS U01 NS052465PHS HHS 1R21-NSO54143
6 · The paper itself

Abstract

Following antigen recognition on target cells, effector T cells establish immunological synapses and secrete cytokines. It is thought that T cells secrete cytokines in one of two modes: either synaptically (i.e., toward antigenic target cells) or multidirectionally, affecting a wider population of cells. This paradigm predicts that synaptically secreted cytokines such as IFN-γ will preferentially signal to antigenic target cells contacted by the T cell through an immunological synapse. Despite its physiological significance, this prediction has never been tested. We developed a live-cell imaging system to compare the responses of target cells and nonantigenic bystanders to IFN-γ secreted by CD8+, antigen-specific, cytotoxic T cells. Both target cells and surrounding nontarget cells respond robustly. This pattern of response was detected even at minimal antigenic T-cell stimulation using low doses of antigenic peptide, or altered peptide ligands. Although cytotoxic immunological synapses restrict killing to antigenic target cells, the effects of IFN-γ are more widespread.

Indexed as

AdenoviridaeAnalysis of VarianceAstrocytesGenetic VectorsGreen Fluorescent ProteinsImage Processing, Computer-AssistedImmunological SynapsesInterferon-gammaMicroscopyT-Lymphocytes, CytotoxicGreen Fluorescent ProteinsInterferon-gamma

Identifiers

PMID22547816
PMCPMC3356634

What OpenQuestion holds

Textmetadata
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.