Altered glycosylation profiles of serum IgG in Takayasu arteritis

Abstract Background Takayasu arteritis (TAK) is an autoimmune inflammatory disorder with an undefined etiology. This study aimed to characterize the glycosylation profiles of serum immunoglobulin G (IgG) in patients with TAK. Methods Lectin microarrays containing 56 types of lectins were used to det...

Full description

Bibliographic Details
Main Authors: Lingyu Liu, Jing Li, Yunjiao Yang, Chaojun Hu, Xinping Tian
Format: Article
Language:English
Published: BMC 2023-02-01
Series:European Journal of Medical Research
Subjects:
Online Access:https://doi.org/10.1186/s40001-023-01035-4
_version_ 1811166019841949696
author Lingyu Liu
Jing Li
Yunjiao Yang
Chaojun Hu
Xinping Tian
author_facet Lingyu Liu
Jing Li
Yunjiao Yang
Chaojun Hu
Xinping Tian
author_sort Lingyu Liu
collection DOAJ
description Abstract Background Takayasu arteritis (TAK) is an autoimmune inflammatory disorder with an undefined etiology. This study aimed to characterize the glycosylation profiles of serum immunoglobulin G (IgG) in patients with TAK. Methods Lectin microarrays containing 56 types of lectins were used to detect the glycan levels of serum IgG in 164 patients with TAK, 128 patients with atherosclerosis used as disease controls (DCs), and 100 healthy controls (HCs). Differentially altered glycosylation patterns between TAK and control groups as well as between TAK subgroups were identified and further validated by lectin blot. The classification performance of the TAK-specific glycosylation change was measured by receiver-operating characteristic (ROC) curve analysis. Results Lectin microarray analysis revealed significantly increased N-Acetylgalactosamine (GalNAc) levels in the TAK group compared to the DC and HC groups (all p < 0.01). For TAK subgroups, significantly decreased mannosylation was observed in patients with active TAK compared to patients with inactive disease (p < 0.01). These differences were validated by lectin blot. In addition, GalNAc levels exhibited a considerable potential for discriminating patients with TAK from patients with atherosclerosis, with an area under the curve of 0.749 (p < 0.001), a sensitivity of 71.7%, and a specificity of 73.8%. Conclusions Serum IgG in patients with TAK displayed disease-specific glycosylation alterations. Aberrant GalNAc glycosylation showed substantial value as a diagnostic biomarker. The potential proinflammatory properties of the abnormal glycans may provide new insights into the role of humoral immunity in the pathogenesis of TAK.
first_indexed 2024-04-10T15:45:37Z
format Article
id doaj.art-aa4c3b5829c14af7beae9352b69c47a5
institution Directory Open Access Journal
issn 2047-783X
language English
last_indexed 2024-04-10T15:45:37Z
publishDate 2023-02-01
publisher BMC
record_format Article
series European Journal of Medical Research
spelling doaj.art-aa4c3b5829c14af7beae9352b69c47a52023-02-12T12:07:30ZengBMCEuropean Journal of Medical Research2047-783X2023-02-012811910.1186/s40001-023-01035-4Altered glycosylation profiles of serum IgG in Takayasu arteritisLingyu Liu0Jing Li1Yunjiao Yang2Chaojun Hu3Xinping Tian4Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of EducationDepartment of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of EducationDepartment of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of EducationDepartment of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of EducationDepartment of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital (PUMCH), Key Laboratory of Rheumatology and Clinical Immunology, Ministry of EducationAbstract Background Takayasu arteritis (TAK) is an autoimmune inflammatory disorder with an undefined etiology. This study aimed to characterize the glycosylation profiles of serum immunoglobulin G (IgG) in patients with TAK. Methods Lectin microarrays containing 56 types of lectins were used to detect the glycan levels of serum IgG in 164 patients with TAK, 128 patients with atherosclerosis used as disease controls (DCs), and 100 healthy controls (HCs). Differentially altered glycosylation patterns between TAK and control groups as well as between TAK subgroups were identified and further validated by lectin blot. The classification performance of the TAK-specific glycosylation change was measured by receiver-operating characteristic (ROC) curve analysis. Results Lectin microarray analysis revealed significantly increased N-Acetylgalactosamine (GalNAc) levels in the TAK group compared to the DC and HC groups (all p < 0.01). For TAK subgroups, significantly decreased mannosylation was observed in patients with active TAK compared to patients with inactive disease (p < 0.01). These differences were validated by lectin blot. In addition, GalNAc levels exhibited a considerable potential for discriminating patients with TAK from patients with atherosclerosis, with an area under the curve of 0.749 (p < 0.001), a sensitivity of 71.7%, and a specificity of 73.8%. Conclusions Serum IgG in patients with TAK displayed disease-specific glycosylation alterations. Aberrant GalNAc glycosylation showed substantial value as a diagnostic biomarker. The potential proinflammatory properties of the abnormal glycans may provide new insights into the role of humoral immunity in the pathogenesis of TAK.https://doi.org/10.1186/s40001-023-01035-4Takayasu arteritisImmunoglobulin GGlycosylationLectin microarray
spellingShingle Lingyu Liu
Jing Li
Yunjiao Yang
Chaojun Hu
Xinping Tian
Altered glycosylation profiles of serum IgG in Takayasu arteritis
European Journal of Medical Research
Takayasu arteritis
Immunoglobulin G
Glycosylation
Lectin microarray
title Altered glycosylation profiles of serum IgG in Takayasu arteritis
title_full Altered glycosylation profiles of serum IgG in Takayasu arteritis
title_fullStr Altered glycosylation profiles of serum IgG in Takayasu arteritis
title_full_unstemmed Altered glycosylation profiles of serum IgG in Takayasu arteritis
title_short Altered glycosylation profiles of serum IgG in Takayasu arteritis
title_sort altered glycosylation profiles of serum igg in takayasu arteritis
topic Takayasu arteritis
Immunoglobulin G
Glycosylation
Lectin microarray
url https://doi.org/10.1186/s40001-023-01035-4
work_keys_str_mv AT lingyuliu alteredglycosylationprofilesofserumiggintakayasuarteritis
AT jingli alteredglycosylationprofilesofserumiggintakayasuarteritis
AT yunjiaoyang alteredglycosylationprofilesofserumiggintakayasuarteritis
AT chaojunhu alteredglycosylationprofilesofserumiggintakayasuarteritis
AT xinpingtian alteredglycosylationprofilesofserumiggintakayasuarteritis