Evidence map›Paper›PMID 22660579›Full record

ArticleNature immunology2012

Photocrosslinkable pMHC monomers stain T cells specifically and cause ligand-bound TCRs to be 'preferentially' transported to the cSMAC.

Jianming Xie, Johannes B Huppa, Evan W Newell, Jun Huang, Peter J R Ebert, Qi-Jing Li, Mark M Davis

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. DNA origami demonstrate the unique stimulatory power of single pMHCs as T cell antigens.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Article
  9. Programmed self-assembly of peptide-major histocompatibility complex for antigen-specific immune modulation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. CD8Current opinion in chemical engineering · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Measuring TCR-pMHC Binding In Situ using a FRET-based Microscopy Assay.Journal of visualized experiments : JoVE · 2015
    Article
  16. Article
  17. Article
  18. Molecular architecture of the αβ T cell receptor-CD3 complex.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Review
  20. Review
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

7 authors at 2 institutions in 1 country.

Jianming XieDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California, USA.
Johannes B Huppa
Evan W Newell
Jun Huang
Peter J R Ebert
Qi-Jing Li
Mark M Davis
Stanford University · USDuke University · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
T CELL RECEPTOR STRUCTURE AND EXPRESSIONR01AI022511 · NIAID · STANFORD UNIVERSITY · PI DAVIS, MARK MORRIS · 1985 to 2014
$3.3M
Regulatory mechanisms of miR-19b, a novel mediator of T cell autoimmunityR01AI091878 · NIAID · DUKE UNIVERSITY · PI LI, QIJING · 2012 to 2016
$1.8M
Howard Hughes Medical InstituteNIAID NIH HHS R01 AI022511NIAID NIH HHS R01 AI091878NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

The binding of T cell antigen receptors (TCRs) to specific complexes of peptide and major histocompatibility complex (pMHC) is typically of very low affinity, which necessitates the use of multimeric pMHC complexes to label T lymphocytes stably. We report here the development of pMHC complexes able to be crosslinked by ultraviolet irradiation; even as monomers, these efficiently and specifically stained cognate T cells. We also used this reagent to probe T cell activation and found that a covalently bound pMHC was more stimulatory than an agonist pMHC on lipid bilayers. This finding suggested that serial engagement of TCRs is dispensable for activation when a substantial fraction of TCRs are stably engaged. Finally, pMHC-bound TCRs were 'preferentially' transported into the central supramolecular activation cluster after activation, which suggested that ligand engagement enabled linkage of the TCR and its associated CD3 signaling molecules to the cytoskeleton.

Indexed as

AnimalsCD3 ComplexCells, CulturedColoring AgentsCross-Linking ReagentsCytoskeletonLymphocyte ActivationMajor Histocompatibility ComplexMiceMice, TransgenicReceptors, Antigen, T-CellSignal TransductionT-LymphocytesCD3 ComplexColoring AgentsCross-Linking ReagentsReceptors, Antigen, T-Cell

Identifiers

PMID22660579
PMCPMC3645478
OpenAlexW2064050383

What OpenQuestion holds

Textmetadata
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.