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Altered glycosylation profiles of serum IgG in Takayasu arteritis
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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906894/ https://www.ncbi.nlm.nih.gov/pubmed/36755310 http://dx.doi.org/10.1186/s40001-023-01035-4 |
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author | Liu, Lingyu Li, Jing Yang, Yunjiao Hu, Chaojun Tian, Xinping |
author_facet | Liu, Lingyu Li, Jing Yang, Yunjiao Hu, Chaojun Tian, Xinping |
author_sort | Liu, Lingyu |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-023-01035-4. |
format | Online Article Text |
id | pubmed-9906894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99068942023-02-08 Altered glycosylation profiles of serum IgG in Takayasu arteritis Liu, Lingyu Li, Jing Yang, Yunjiao Hu, Chaojun Tian, Xinping Eur J Med Res Research 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-023-01035-4. BioMed Central 2023-02-08 /pmc/articles/PMC9906894/ /pubmed/36755310 http://dx.doi.org/10.1186/s40001-023-01035-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Lingyu Li, Jing Yang, Yunjiao Hu, Chaojun Tian, Xinping Altered glycosylation profiles of serum IgG in Takayasu arteritis |
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 | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9906894/ https://www.ncbi.nlm.nih.gov/pubmed/36755310 http://dx.doi.org/10.1186/s40001-023-01035-4 |
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