Machine learning analysis of the T cell receptor repertoire identifies sequence features of self-reactivity.
CD4 T cells
CD5
CDR3 beta chain
T cell receptor
chronic infection
heterogeneity
machine learning
retrogenic mice
self-reactivity
thymic development
Journal
Cell systems
ISSN: 2405-4720
Titre abrégé: Cell Syst
Pays: United States
ID NLM: 101656080
Informations de publication
Date de publication:
28 Nov 2023
28 Nov 2023
Historique:
received:
27
05
2023
revised:
01
09
2023
accepted:
09
11
2023
medline:
8
12
2023
pubmed:
8
12
2023
entrez:
7
12
2023
Statut:
aheadofprint
Résumé
The T cell receptor (TCR) determines specificity and affinity for both foreign and self-peptides presented by the major histocompatibility complex (MHC). Although the strength of TCR interactions with self-pMHC impacts T cell function, it has been challenging to identify TCR sequence features that predict T cell fate. To discern patterns distinguishing TCRs from naive CD4
Identifiants
pubmed: 38061355
pii: S2405-4712(23)00327-7
doi: 10.1016/j.cels.2023.11.004
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests The authors declare no competing interests.