Immunopathogenesis of Primary Biliary Cholangitis, Primary Sclerosing Cholangitis and Autoimmune Hepatitis: Themes and Concepts.
Dysbiosis
Epidemiology
Homing
Tolerance
Transplantation
bile acids
fibrosis
genetics
microbiome
Journal
Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630
Informations de publication
Date de publication:
09 Feb 2024
09 Feb 2024
Historique:
received:
25
04
2023
revised:
21
01
2024
accepted:
28
01
2024
medline:
12
2
2024
pubmed:
12
2
2024
entrez:
11
2
2024
Statut:
aheadofprint
Résumé
Autoimmune liver diseases (AILDs) include primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC) and autoimmune hepatitis (AIH), a family of chronic immune-mediated disorders that target hepatocytes and cholangiocytes. Treatments remain non-specific, variably effective and non-curative, and the need for liver transplantation is disproportionate to their rarity. Development of effective therapies requires better knowledge of pathogenic mechanisms, including the roles of genetic risk, and how the environment and gut dysbiosis cause immune cell dysfunction and aberrant bile acid signalling. This review summarises key aetiolopathogenic concepts and themes relevant for clinical practice, and how such learnings can guide the development of new therapies for people living with AILDs.
Identifiants
pubmed: 38342195
pii: S0016-5085(24)00165-3
doi: 10.1053/j.gastro.2024.01.049
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 AGA Institute. Published by Elsevier Inc. All rights reserved.