Authors
Franco Vukovic
Jasminka Krištić
Ivan Gudelj
Maria Teruel
Toma Keser
Marija Pezer
Maja Pučić-Baković
Jerko Štambuk
Irena Trbojević-Akmačić
Clara Barrios
Tamara Pavić
Cristina Menni
Youxin Wang
Yong Zhou
Liufu Cui
Haicheng Song
Qiang Zeng
Xiuhua Guo
Bernardo A. Pons-Estel
Paul McKeigue
Alan Leslie Patrick
Olga Gornik
Tim D. Spector
Miroslav Harjaček
Marta Alarcon-Riquelme
Miriam Molokhia
Wei Wang, Edith Cowan UniversityFollow
Gordan Lauc
Document Type
Journal Article
Publisher
John Wiley and Sons, Inc
Place of Publication
United States
Faculty
Faculty of Health, Engineering and Science
School
School of Medical and Health Sciences
RAS ID
19925
Abstract
Objective: Glycans attached to the Fc portion of IgG are important modulators of IgG effector functions. Interindividual differences in IgG glycome composition are large and they associate strongly with different inflammatory and autoimmune diseases. IKZF1, HLA–DQ2A/B, and BACH2 genetic loci that affect IgG glycome composition show pleiotropy with systemic lupus erythematosus (SLE), indicating a potentially causative role of aberrant IgG glycosylation in SLE. We undertook this large multicenter case–control study to determine whether SLE is associated with altered IgG glycosylation. Methods: Using ultra-performance liquid chromatography analysis of released glycans, we analyzed the composition of the IgG glycome in 261 SLE patients and 247 matched controls of Latin American Mestizo origin (the discovery cohort) and in 2 independent replication cohorts of different ethnicity (108 SLE patients and 193 controls from Trinidad, and 106 SLE patients and 105 controls from China). Results: Multiple statistically significant differences in IgG glycome composition were observed between patients and controls. The most significant changes included decreased galactosylation and sialylation of IgG (which regulate proinflammatory and antiinflammatory actions of IgG) as well as decreased core fucose and increased bisecting N-acetylglucosamine (which affect antibody-dependent cell-mediated cytotoxicity). Conclusion: The IgG glycome in SLE patients is significantly altered in a way that decreases immunosuppressive action of circulating immunoglobulins. The magnitude of observed changes is associated with the intensity of the disease, indicating that aberrant IgG glycome composition or changes in IgG glycosylation may be an important molecular mechanism in SLE.
DOI
10.1002/art.39273
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
Comments
Vučković, F., Krištić, J., Gudelj, I., Teruel, M., Keser, T., Pezer, M., ...Lauc, G. (2015). Association of systemic lupus erythematosus associates with decreased immunosuppressive potential of the IgG glycome. Arthritis & Rheumatology, 67(11), 2978-2989. Available here