Evidence map›Paper›PMID 37459191›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2023

What's the Catch? The Significance of Catch Bonds in T Cell Activation.

Michael A Faust, Viva J Rasé, Tracey J Lamb, Brian D Evavold

Open access · greenAbstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. 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

4 authors at 1 institution in 1 country.

Michael A FaustDivision of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT.ORCID 0000-0002-3185-2850
Viva J RaséDivision of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT.ORCID 0000-0001-7314-8899
Tracey J LambDivision of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT.ORCID 0000-0003-0620-3944
Brian D EvavoldDivision of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT.ORCID 0000-0002-3561-3494
University of Utah · US

Funding

CD4+ T cell affinity for self and foreign antigens in the CNSR01NS071518 · NINDS · UNIVERSITY OF UTAH · PI EVAVOLD, BRIAN D · 2010 to 2021
$3.3M
CD8 T cell antigen recognition during chronic infectionR01AI147641 · NIAID · UNIVERSITY OF UTAH · PI EVAVOLD, BRIAN D · 2020 to 2024
$3.3M
Pathogenic low affinity CD8 T cells in malariaR01AI167422 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI EVAVOLD, BRIAN D, LAMB, TRACEY JANE · 2021 to 2025
$3.3M
Defining how TCR strength of signal modulates Treg functionR01AI169835 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Brian D Evavold · 2022 to 2026
$3.1M
Cross-disciplinary Training in Immunology, Inflammation and Infectious DiseaseT32AI138945 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Tracey Jane Lamb, Matthew A Williams · 2018 to 2026
$1.6M
The Neuroimmunology Training Program at the University of UtahT32NS115664 · NINDS · UNIVERSITY OF UTAH · PI O'CONNELL, RYAN M, WILCOX, KAREN S · 2020 to 2024
$988k
NIAID NIH HHS R01 AI147641NIAID NIH HHS R01 AI167422NIAID NIH HHS R01 AI169835NIAID NIH HHS T32 AI138945NINDS NIH HHS R01 NS071518NINDS NIH HHS T32 NS115664
6 · The paper itself

Abstract

One of the main goals in T cell biology has been to investigate how TCR recognition of peptide:MHC (pMHC) determines T cell phenotype and fate. Ag recognition is required to facilitate survival, expansion, and effector function of T cells. Historically, TCR affinity for pMHC has been used as a predictor for T cell fate and responsiveness, but there have now been several examples of nonfunctional high-affinity clones and low-affinity highly functional clones. Recently, more attention has been paid to the TCR being a mechanoreceptor where the key biophysical determinant is TCR bond lifetime under force. As outlined in this review, the fundamental parameters between the TCR and pMHC that control Ag recognition and T cell triggering are affinity, bond lifetime, and the amount of force at which the peak lifetime occurs.

Indexed as

Receptors, Antigen, T-CellT-LymphocytesClone CellsLymphocyte ActivationProtein BindingReceptors, Antigen, T-Cell

Identifiers

PMID37459191
PMCPMC10732538
OpenAlexW4384575932

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.