Evidence map›Paper›PMID 26284470›Full record

ReviewImmunological reviews2015

Coevolution of T-cell receptors with MHC and non-MHC ligands.

Caitlin D Castro, Adrienne M Luoma, Erin J Adams

Abstract readReview
In one paragraph

Review in Immunological reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  17. Observational
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  19. Review
  20. TRAV7-2*02 Expressing CD8⁺ T Cells Are Responsible for Palladium Allergy.International journal of molecular sciences · 2017
    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 1 institution in 1 country.

Caitlin D CastroDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Adrienne M LuomaDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Erin J AdamsDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
University of Chicago · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
RESEARCH TRAINING IN RESPIRATORY BIOLOGYT32HL007605 · NHLBI · UNIVERSITY OF CHICAGO · PI Yun Fang, Gokhan M. Mutlu · 1985 to 2026
$18.1M
Molecular Recognition of Ligand by the Gamma Delta T Cell ReceptorR01AI073922 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2007 to 2016
$3.8M
Gamma Delta T cell surveillance of metabolites as signals of cellular stressR01AI115471 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2015 to 2019
$1.9M
NCATS NIH HHS UL1 TR000430NHLBI NIH HHS T32 HL007605NIAID NIH HHS R01 AI073922NIAID NIH HHS R01AI073922NIAID NIH HHS R01 AI115471NIAID NIH HHS R01AI115471
6 · The paper itself

Abstract

The structure and amino acid diversity of the T-cell receptor (TCR), similar in nature to that of Fab portions of antibodies, would suggest that these proteins have a nearly infinite capacity to recognize antigen. Yet all currently defined native T cells expressing an α and β chain in their TCR can only sense antigen when presented in the context of a major histocompatibility complex (MHC) molecule. This MHC molecule can be one of many that exist in vertebrates, presenting small peptide fragments, lipid molecules, or small molecule metabolites. Here we review the pattern of TCR recognition of MHC molecules throughout a broad sampling of species and T-cell lineages and also touch upon T cells that do not appear to require MHC presentation for their surveillance function. We review the diversity of MHC molecules and information on the corresponding T-cell lineages identified in divergent species. We also discuss TCRs with structural domains unlike that of conventional TCRs of mouse and human. By presenting this broad view of TCR sequence, structure, domain organization, and function, we seek to explore how this receptor has evolved across time and been selected for alternative antigen-recognition capabilities in divergent lineages.

Indexed as

AnimalsEvolution, MolecularHumansLigandsMajor Histocompatibility ComplexModels, MolecularProtein BindingProtein Structure, TertiaryReceptors, Antigen, T-CellT-LymphocytesLigandsReceptors, Antigen, T-CellevolutionMHCMHC-like class Inon-classical class IstructureTCR recognition

Identifiers

PMID26284470
PMCPMC4544829
OpenAlexW1919861825

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.