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
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

110266

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Silvia Sartoris (S)

Dept. of Medicine, Section of Immunology University of Verona School of Medicine, Verona, Italy.

Giovanna Del Pozzo (G)

Institute of Genetics and Biophysics "Adriano Buzzati Traverso" National Research Council (CNR), Naples, Italy.

Classifications MeSH