Evidence map›Paper›PMID 15980863›Full record

ArticleNature immunology2005

Nonstimulatory peptides contribute to antigen-induced CD8-T cell receptor interaction at the immunological synapse.

Pia P Yachi, Jeanette Ampudia, Nicholas R J Gascoigne, Tomasz Zal

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

76 citing papers in PubMed, 125 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. T cell receptor (TCR) signaling in health and disease.Signal transduction and targeted therapy · 2021
    Review
  7. Article
  8. Article
  9. The transcription factor Zfp281 sustains CD4Cellular & molecular immunology · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Sex bias in MHC I-associated shaping of the adaptive immune system.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Review
  16. Review
  17. Article
  18. Understanding FRET as a research tool for cellular studies.International journal of molecular sciences · 2015
    Review
  19. Article
  20. Article

16 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

4 authors at 1 institution in 1 country.

Pia P YachiDepartment of Immunology, IMM1, The Scripps Research Institute, La Jolla, California 92037, USA.
Jeanette Ampudia
Nicholas R J Gascoigne
Tomasz Zal
Scripps Research Institute · US

Funding

Therapeutics Core (Page 286)P30MH062261 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GENDELMAN, HOWARD E · 2000 to 2021
$37.7M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
PATHOGENESIS AND IMMUNOLOGY OF DISEASET32AI007244 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 1985 to 2022
$8.8M
Intermolecular Interactions in the Immunological SynapseR01GM065230 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SAUER, KARSTEN · 2002 to 2014
$4.6M
SOLUBLE T CELL RECEPTOR STUDIES ON MHC RESTRICTIONSR01GM039476 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI GASCOIGNE, NICHOLAS R · 1995 to 2006
$2.2M
Real-time molecular interactions in tolerance inductionR21DK061329 · NIDDK · SCRIPPS RESEARCH INSTITUTE · PI GASCOIGNE, NICHOLAS R · 2001 to 2003
$822k
SOLUBLE T CELL RECEPTOR STUDIES ON MHC RESTRICTIONR29GM039476 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI GASCOIGNE, NICHOLAS R · 1988 to 1992
–
NIAID NIH HHS T32 AI007244NIAID NIH HHS T32 AI007290NIAID NIH HHS T32 AI07290NIDDK NIH HHS DK61329NIDDK NIH HHS R21 DK061329NIGMS NIH HHS GM039476NIGMS NIH HHS GM065230NIGMS NIH HHS R01 GM039476NIGMS NIH HHS R01 GM065230NIMH NIH HHS P30 MH062261NIMH NIH HHS P30MH62261
6 · The paper itself

Abstract

It is unclear if the interaction between CD8 and the T cell receptor (TCR)-CD3 complex is constitutive or antigen induced. Here, fluorescence resonance energy transfer microscopy between fluorescent chimeras of CD3zeta and CD8beta showed that this interaction was induced by antigen recognition in the immunological synapse. Nonstimulatory endogenous or exogenous peptides presented simultaneously with antigenic peptides increased the CD8-TCR interaction. This finding indicates that the interaction between the intracellular regions of a TCR-CD3 complex recognizing its cognate peptide-major histocompatibility complex (MHC) antigen, and CD8 (plus the kinase Lck), is enhanced by a noncognate CD8-MHC interaction. Thus, the interaction of CD8 with a nonstimulatory peptide-MHC complex helps mediate T cell recognition of antigen, improving the coreceptor function of CD8.

Indexed as

AlgorithmsAmino Acid MotifsAntigensBacterial ProteinsCD3 ComplexCD8 AntigensCD8-Positive T-LymphocytesCell CommunicationDose-Response Relationship, DrugDown-RegulationFlow CytometryFluorescence Resonance Energy TransferGreen Fluorescent ProteinsHumansHybridomasImmunoblottingAntigensBacterial ProteinsCD3 antigen, zeta chainCD3 ComplexCD8 AntigensCyan Fluorescent ProteinGreen Fluorescent ProteinsLuminescent ProteinsPeptidesReceptors, Antigen, T-CellRecombinant Fusion ProteinsTyrosineyellow fluorescent protein, Bacteria

Identifiers

PMID15980863
PMCPMC1352171
OpenAlexW2057801890

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.