Glycan biomarkers of autoimmunity and bile acid-associated alterations of the human glycome: Primary biliary cirrhosis and primary sclerosing cholangitis-specific glycans.
Autoimmunity
B-Lymphocytes
/ immunology
Bile Acids and Salts
/ blood
Biomarkers
/ blood
Case-Control Studies
Cholangitis, Sclerosing
/ blood
Diagnosis, Differential
Glycomics
/ methods
Glycopeptides
/ blood
Glycosylation
Humans
Liver Cirrhosis, Biliary
/ blood
Polysaccharides
/ blood
Spectrometry, Mass, Electrospray Ionization
/ methods
Multiple Reaction Monitoring
N-glycopeptides
Primary Biliary Cirrhosis (PBC)
Primary Sclerosing Cholangitis (PSC)
biomarker testing
plasma
Journal
Clinical immunology (Orlando, Fla.)
ISSN: 1521-7035
Titre abrégé: Clin Immunol
Pays: United States
ID NLM: 100883537
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
received:
27
01
2021
revised:
10
08
2021
accepted:
11
08
2021
pubmed:
18
8
2021
medline:
14
9
2021
entrez:
17
8
2021
Statut:
ppublish
Résumé
We have recently introduced multiple reaction monitoring (MRM) mass spectrometry as a novel tool for glycan biomarker research and discovery. Herein, we employ this technique to characterize the site-specific glycan alterations associated with primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC). Glycopeptides associated with disease severity were also identified. Multinomial regression modelling was employed to construct and validate multi-analyte diagnostic models capable of accurately distinguishing PBC, PSC, and healthy controls from one another (AUC = 0.93 ± 0.03). Finally, to investigate how disease-relevant environmental factors can influence glycosylation, we characterized the ability of bile acids known to be differentially expressed in PBC to alter glycosylation. We hypothesize that this could be a mechanism by which altered self-antigens are generated and become targets for immune attack. This work demonstrates the utility of the MRM method to identify diagnostic site-specific glycan classifiers capable of distinguishing even related autoimmune diseases from one another.
Identifiants
pubmed: 34403816
pii: S1521-6616(21)00162-5
doi: 10.1016/j.clim.2021.108825
pii:
doi:
Substances chimiques
Bile Acids and Salts
0
Biomarkers
0
Glycopeptides
0
Polysaccharides
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
108825Subventions
Organisme : NIH HHS
ID : DP2 OD008752
Pays : United States
Informations de copyright
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.