Evidence map›Paper›PMID 28771705›Full record

ReviewImmunology2018

Selected signalling proteins recruited to the T-cell receptor-CD3 complex.

Jatuporn Ngoenkam, Wolfgang W Schamel, Sutatip Pongcharoen

Open access · bronzeAbstract readReview
In one paragraph

Review in Immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

50 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Identification of Novel Kv1.3 Channel-Interacting Proteins Using Proximity Labelling in T-Cells.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Lymph-Node-Based CD3Journal of virology · 2023
    Article
  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

3 authors at 2 institutions in 2 countries.

Jatuporn NgoenkamDepartment of Microbiology and Parasitology, Faculty of Medical Science, Naresuan University, Phitsanulok, Thailand.ORCID 0000-0002-3762-3872
Wolfgang W SchamelDepartment of Immunology, Institute for Biology III, Faculty of Biology, University of Freiburg, Freiburg, Germany.
Sutatip PongcharoenCentre of Excellence in Medical Biotechnology, Faculty of Medical Science, Naresuan University, Phitsanulok, Thailand.
Naresuan University · THUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The T-cell receptor (TCR)-CD3 complex, expressed on T cells, determines the outcome of a T-cell response. It consists of the TCR-αβ heterodimer and the non-covalently associated signalling dimers of CD3εγ, CD3εδ and CD3ζζ. TCR-αβ binds specifically to a cognate peptide antigen bound to an MHC molecule, whereas the CD3 subunits transmit the signal into the cytosol to activate signalling events. Recruitment of proteins to specialized localizations is one mechanism to regulate activation and termination of signalling. In the last 25 years a large number of signalling molecules recruited to the TCR-CD3 complex upon antigen binding to TCR-αβ have been described. Here, we review knowledge about five of those interaction partners: Lck, ZAP-70, Nck, WASP and Numb. Some of these proteins have been targeted in the development of immunomodulatory drugs aiming to treat patients with autoimmune diseases and organ transplants.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCD3 ComplexHumansLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsMutationNerve Tissue ProteinsOncogene ProteinsProtein BindingProtein Interaction Domains and MotifsReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-CellT-Lymphocyte SubsetsAdaptor Proteins, Signal TransducingCarrier ProteinsCD3 ComplexLymphocyte Specific Protein Tyrosine Kinase p56(lck)Membrane ProteinsNck proteinNerve Tissue ProteinsNUMB protein, humanOncogene ProteinsReceptor-CD3 Complex, Antigen, T-CellReceptors, Antigen, T-CellWiskott-Aldrich Syndrome ProteinZAP-70 Protein-Tyrosine Kinaseprotein-protein interactionsignal transductionT-cell activationT-cell receptor-CD3 complex

Identifiers

PMID28771705
PMCPMC5721247
OpenAlexW2745126636

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.