Presence of antibodies to native G1 domain of aggrecan core protein in synovial fluids from patients with various joint diseases

被引:30
作者
Karopoulos, C
Rowley, MJ
Ilic, MZ
Handley, CJ
机构
[1] MONASH UNIV,CLAYTON,VIC 3168,AUSTRALIA
[2] LA TROBE UNIV,BUNDOORA,VIC 3083,AUSTRALIA
来源
ARTHRITIS AND RHEUMATISM | 1996年 / 39卷 / 12期
关键词
D O I
10.1002/art.1780391207
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate the occurrence of IgG antibodies to aggrecan in synovial fluids (SF) from patients with arthritis and various articular diseases, and to determine the nature of epitopes present within aggrecan that react with these antibodies. Methods. SF samples were reacted with native aggrecan, reduced and alkylated aggrecan, chondroitin sulfate, and keratan sulfate, using dot-blots and a novel enzyme-linked immunosorbent assay (ELISA), The nature of the epitopes present on aggrecan was elucidated using Western blots and a competitive inhibition ELISA. Results. IgG antibodies to aggrecan were found in >50% of the SF samples tested. No IgG antibody reactivity was observed in serum from the same patients, The antibodies appeared to react predominantly with native aggrecan, and there was no disease specificity, It was shown that the epitopes to these antibodies were located within the N-terminal region of the core protein. Conclusion. This study demonstrates the frequent occurrence of IgG antibodies to aggrecan in human SF. The major epitope is located in the G1 domain of the aggrecan core protein, These IgG antibodies appear to be produced locally within the synovial cavity, probably in response to various articular diseases, resulting in the loss of native aggrecan from articular cartilage.
引用
收藏
页码:1990 / 1997
页数:8
相关论文
共 38 条
[1]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]  
CALABRO A, 1992, ARCH BIOCHEM BIOPHYS, V258, P143
[4]  
CATERSON B, 1985, FED PROC, V44, P386
[5]  
CHAMPION BR, 1981, COLLAGEN REL RES, V1, P453
[6]  
DOEGE K, 1987, J BIOL CHEM, V262, P17757
[7]  
DOEGE KJ, 1991, J BIOL CHEM, V266, P894
[8]  
EYRE DR, 1991, J RHEUMATOL, V18, P49
[9]   IMPROVED QUANTITATION AND DISCRIMINATION OF SULFATED GLYCOSAMINOGLYCANS BY USE OF DIMETHYLMETHYLENE BLUE [J].
FARNDALE, RW ;
BUTTLE, DJ ;
BARRETT, AJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 883 (02) :173-177
[10]   IMMUNOPATHOLOGIC ROLE OF PROTEOGLYCAN ANTIGENS IN RHEUMATOID JOINT DISEASE [J].
GLANT, T ;
CSONGOR, J ;
SZUCS, T .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1980, 11 (03) :247-252