Exploring the HLA complex in autoimmunity: From the risk haplotypes to the modulation of expression.
Autoimmune disease
Gene expression
HLA
Haplotype
Self-antigen
Journal
Clinical immunology (Orlando, Fla.)
ISSN: 1521-7035
Titre abrégé: Clin Immunol
Pays: United States
ID NLM: 100883537
Informations de publication
Date de publication:
06 Jun 2024
06 Jun 2024
Historique:
received:
24
04
2024
revised:
29
05
2024
accepted:
30
05
2024
medline:
9
6
2024
pubmed:
9
6
2024
entrez:
8
6
2024
Statut:
aheadofprint
Résumé
The genes mapping at the HLA region show high density, strong linkage disequilibrium and high polymorphism, which affect the association of HLA class I and class II genes with autoimmunity. We focused on the HLA haplotypes, genomic structures consisting of an array of specific alleles showing some degrees of genetic association with different autoimmune disorders. GWASs in many pathologies have identified variants in either the coding loci or the flanking regulatory regions, both in linkage disequilibrium in haplotypes, that are frequently associated with increased risk and may influence gene expression. We discuss the relevance of the HLA gene expression because the level of surface heterodimers determines the number of complexes presenting self-antigen and, thus, the strength of pathogenic autoreactive T cells immune response.
Identifiants
pubmed: 38851519
pii: S1521-6616(24)00375-9
doi: 10.1016/j.clim.2024.110266
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
110266Informations de copyright
Copyright © 2024. Published by Elsevier Inc.