Reduced systemic IgG levels against peptidoglycan in rheumatoid arthritis (RA) patients

被引:14
作者
Schrijver, IA
De Man, YA
Melief, MJ
Van Laar, JM
Markusse, HM
Klasen, IS
Hazenberg, MP
Laman, JD
机构
[1] Erasmus Univ, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
[2] Univ Hosp Dijkzigt, NL-3015 GD Rotterdam, Netherlands
[3] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
[4] Zuiderziekenhuis, Dept Rheumatol, Rotterdam, Netherlands
[5] Univ Nijmegen, St Radboud Hosp, Dept Clin Chem, Nijmegen, Netherlands
关键词
Gram-positive bacteria; gut flora; rheumatoid arthritis; antibodies; peptidoglycan;
D O I
10.1046/j.1365-2249.2001.01419.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gut flora is believed to play a role in the pathogenesis of RA. Peptidoglycan, a major cell wall component of Gram-positive bacteria, is a candidate antigen because of its capability to trigger production of proinflammatory cytokines, to induce arthritis in rodents, and because of its presence in antigen-presenting cells in RA joints. We investigated whether the systemic and local antibody levels against a peptidoglycan-polysaccharide (PG-PS) are related to the presence and disease activity of RA. Significantly lower levels of systemic IgG directed against PG-PS were found in healthy females compared with healthy males, and systemic IgA levels specific for PG-PS were negatively correlated with age. Levels of systemic IgG directed against PG-PS were significantly reduced in RA patients compared with sex- and age-matched healthy controls. Local (synovial fluid) levels of IgG did not correlate with disease activity whereas synovial fluid levels of IgA correlated positively with disease activity. These data suggest that IgG in healthy people mediates protection against spreading of PG to non-mucosal sites.
引用
收藏
页码:140 / 146
页数:7
相关论文
共 47 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]  
Brandtzaeg P, 1997, ALIMENT PHARM THER, V11, P24
[3]   Regional specialization in the mucosal immune system: what happens in the microcompartments? [J].
Brandtzaeg, P ;
Baekkevold, ES ;
Farstad, IN ;
Jahnsen, FL ;
Johansen, FE ;
Nilsen, EM ;
Yamanaka, T .
IMMUNOLOGY TODAY, 1999, 20 (03) :141-151
[4]   Regional specialization in the mucosal immune system: primed cells do not always home along the same track [J].
Brandtzaeg, P ;
Farstad, IN ;
Haraldsen, G .
IMMUNOLOGY TODAY, 1999, 20 (06) :267-277
[5]  
De Vos M, 1998, ALIMENT PHARM THERAP, V12, P397
[6]   Role of cytokines in rheumatoid arthritis [J].
Feldmann, M ;
Brennan, FM ;
Maini, RN .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :397-440
[7]  
GASTON JSH, 1995, BRIT J RHEUMATOL, V34, P801
[8]  
GASTON JSH, 1989, CLIN EXP IMMUNOL, V76, P348
[9]   SALMONELLA LIPOPOLYSACCHARIDE IN SYNOVIAL-CELLS FROM PATIENTS WITH REACTIVE ARTHRITIS [J].
GRANFORS, K ;
JALKANEN, S ;
LINDBERG, AA ;
MAKIIKOLA, O ;
VONESSEN, R ;
LAHESMAARANTALA, R ;
ISOMAKI, H ;
SAARIO, R ;
ARNOLD, WJ ;
TOIVANEN, A .
LANCET, 1990, 335 (8691) :685-688
[10]   YERSINIA-ENTEROCOLITICA IN THE SYNOVIAL-MEMBRANE OF PATIENTS WITH YERSINIA-INDUCED ARTHRITIS [J].
HAMMER, M ;
ZEIDLER, H ;
KLIMSA, S ;
HEESEMANN, J .
ARTHRITIS AND RHEUMATISM, 1990, 33 (12) :1795-1800