Measuring decreased serum IgG sialylation: a novel clinical biomarker of lupus

被引:14
作者
Chen, X-X [1 ]
Chen, Y-Q [1 ]
Ye, S. [1 ]
机构
[1] Jiaotong Univ, Dept Rheumatol, Renji Hosp, Sch Med, Shanghai, Peoples R China
关键词
Sialylation of immunoglobulin G; autoimmune diseases; ELISA assay; SITE-SPECIFIC GLYCOSYLATION; IMMUNOGLOBULIN-G; POLYSIALIC ACID; ANTIINFLAMMATORY ACTIVITY; INFLAMMATORY DISEASES; RHEUMATOID-ARTHRITIS; FC-SIALYLATION; OLIGOSACCHARIDES; COMPLEMENT; CHALLENGES;
D O I
10.1177/0961203315570686
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction The aim of this work was to develop a simple assay to distinguish between patients with rheumatoid arthritis (RA) and patients with systemic lupus erythematosus (SLE) by measuring the serum sialylated IgG (SAIgG). Methods Using a newly established SNA-based ELISA method, we compared the sialylation of immunoglobulin G (IgG) from a healthy control group (n=41), RA patients (n=30), SLE patients (n=45), patients with neuropsychiatric SLE (NPSLE) (n=30) and patients with juvenile idiopathic arthritis (JIA) (n=32). Results The average SAIgG level in healthy control individuals, RA patients, JIA patients, SLE patients and NPSLE patients was 0.640.17, 0.82 +/- 0.33, 0.69 +/- 0.23, 0.12 +/- 0.02 and 0.03 +/- 0.01mg/ml, respectively. The ratio of sialylated IgG to total IgG was significantly decreased in the SLE group (1.88 +/- 0.32%) compared with the healthy population (4.64 +/- 0.90%). Conclusion In summary, while the mean serum SAIgG level of RA and JIA patients was similar to that of the healthy population, there was a significant decrease in the serum SAIgG of both SLE groups tested, whereby the level of the NPSLE population group was the lowest.
引用
收藏
页码:948 / 954
页数:7
相关论文
共 28 条
[1]
Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG fc [J].
Anthony, Robert M. ;
Nimmerjahn, Falk ;
Ashline, David J. ;
Reinhold, Vernon N. ;
Paulson, James C. ;
Ravetch, Jeffrey V. .
SCIENCE, 2008, 320 (5874) :373-376
[2]
Novel roles for the IgG Fc glycan [J].
Anthony, Robert M. ;
Wermeling, Fredrik ;
Ravetch, Jeffrey V. .
GLYCOBIOLOGY OF THE IMMUNE RESPONSE, 2012, 1253 :170-180
[3]
CHANGES IN NORMAL GLYCOSYLATION MECHANISMS IN AUTOIMMUNE RHEUMATIC DISEASE [J].
AXFORD, JS ;
SUMAR, N ;
ALAVI, A ;
ISENBERG, DA ;
YOUNG, A ;
BODMAN, KB ;
ROITT, IM .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (03) :1021-1031
[4]
Roles, regulation, and mechanism of polysialic acid function during neural development [J].
Brusés, JL ;
Rutishauser, U .
BIOCHIMIE, 2001, 83 (07) :635-643
[5]
Alteration of neural tissue structure by expression of polysialic acid induced by viral delivery of PST polysialyltransferase [J].
Canger, AK ;
Rutishauser, U .
GLYCOBIOLOGY, 2004, 14 (01) :83-93
[6]
Sialylated therapeutic IgG:: a sweet remedy for inflammatory diseases? [J].
Dimitrov, Jordan D. ;
Bayry, Jagadeesh ;
Siberil, Sophie ;
Kaveri, Srini V. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (05) :1301-1304
[7]
Down-regulation of polysialic acid is required for efficient myelin formation [J].
Fewou, Simon Ngamli ;
Ramakrishnan, Hariharasubramanian ;
Buessow, Heinrich ;
Gieselmann, Volkmar ;
Eckhardt, Matthias .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (22) :16700-16711
[8]
Polysialylated neural cell adhesion molecule is necessary for selective targeting of regenerating motor neurons [J].
Franz, CK ;
Rutishauser, U ;
Rafuse, VF .
JOURNAL OF NEUROSCIENCE, 2005, 25 (08) :2081-2091
[9]
Analysis and Functional Consequences of Increased Fab-Sialylation of Intravenous Immunoglobulin (IVIG) after Lectin Fractionation [J].
Kaesermann, Fabian ;
Boerema, David J. ;
Rueegsegger, Monika ;
Hofmann, Andreas ;
Wymann, Sandra ;
Zuercher, Adrian W. ;
Miescher, Sylvia .
PLOS ONE, 2012, 7 (06)
[10]
Anti-inflammatory activity of immunoglobulin G resulting from Fc sialylation [J].
Kaneko, Yoshikatsu ;
Nimmerjahn, Falk ;
Ravetch, Jeffrey V. .
SCIENCE, 2006, 313 (5787) :670-673