Levels of antibodies against Clq and 60 kDa family of heat shock proteins in the sera of patients with various autoimmune diseases

被引:31
作者
Horváth, L
Czirják, L
Fekete, B
Jakab, L
Prohászka, Z
Cervenak, L
Romics, L
Singh, M
Daha, MR
Füst, G
机构
[1] Semmelweis Univ, Fac Med, Dept Med 3, H-1125 Budapest, Hungary
[2] Hungarian Acad Sci, Res Grp Metab Genet & Immunol, Budapest, Hungary
[3] Univ Pecs, Fac Med, Nephrol Ctr, Pecs, Hungary
[4] Univ Pecs, Fac Med, Dept Internal Med 2, Pecs, Hungary
[5] German Natl Res Ctr Biotechnol, Braunschweig, Germany
[6] Univ Leiden Hosp, Dept Nephrol, NL-2300 RC Leiden, Netherlands
关键词
Clq; heat shock proteins; autoimmune disease; systemic lupus erythematosus;
D O I
10.1016/S0165-2478(00)00287-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
Previously a strong positive correlation was found between antibodies to Clq (ClqAb) and antibodies against human heat shock protein (hsp60) and mycobacterial hsp65 in HIV infected patients. Here the levels of these antibodies were measured in the sera of patients with different autoimmune diseases (123 systemic lupus erythematosus (SLE), 55 systemic sclerosis, 33 undifferentiated connective tissue disease (UCTD), 27 primary Raynaud syndrome, 21 rheumatoid arthritis (RA). 14 polymyositis/dermatomyositis (PM/DM), and 192 healthy blood donors. The prevalence of Ige ClqAb was found to be high (P < 0.0001 as compared to the healthy controls) only in the SLE group. The levels of the anti-hsp60 (P = 0.0094) and anti-hsp65 (P = 0.0108) antibodies were high only in the UCTD patients. No correlation was found between the ClqAb and anti-hsp antibodies in any group except a significant (P = 0.011) positive correlation between ClqAb and hsp65 antibodies in the patients with UCTD. These findings indicate that the autoantibodies against Clq are heterogeneous: in different diseases different types of ClqAb may dominate. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 35 条
[1]  
ALARCON GS, 1991, J RHEUMATOL, V18, P1332
[2]  
ALEN JC, 1996, J RHEUMATOL, V23, P469
[3]   PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SYSTEMIC-SCLEROSIS (SCLERODERMA) [J].
不详 .
ARTHRITIS AND RHEUMATISM, 1980, 23 (05) :581-590
[4]   Association between antibodies to heat shock protein 65 and coronary atherosclerosis - Possible mechanism of action of Helicobacter pylori and other bacterial infections in increasing cardiovascular risk [J].
Birnie, DH ;
Holme, ER ;
McKay, IC ;
Hood, S ;
McColl, KEL ;
Hillis, WS .
EUROPEAN HEART JOURNAL, 1998, 19 (03) :387-394
[5]  
CalvoAlen J, 1996, J RHEUMATOL, V23, P469
[6]   THE COGNITIVE PARADIGM AND THE IMMUNOLOGICAL HOMUNCULUS [J].
COHEN, IR .
IMMUNOLOGY TODAY, 1992, 13 (12) :490-494
[7]  
Danieli MG, 1999, CLIN EXP RHEUMATOL, V17, P585
[8]   Autoantibodies to the collagen-like region of C1q are strongly associated with classical pathway-mediated hypocomplementemia in systemic lupus erythematosus [J].
FremeauxBacchi, V ;
Weiss, L ;
Demouchy, C ;
Blouin, J ;
Kazatchkine, MD .
LUPUS, 1996, 5 (03) :216-220
[9]   Increased antibody titers against mycobacterial heat-shock protein 65 in patients with vasculitis and arteriosclerosis [J].
Gruber, R ;
Lederer, S ;
Bechtel, U ;
Lob, S ;
Riethmuller, G ;
Feucht, HE .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1996, 110 (01) :95-98
[10]   Preferential binding with Escherichia coli hsp60 of antibodies prevalent in sera from patients with rheumatoid arthritis [J].
Hirata, D ;
Hirai, I ;
Iwamoto, M ;
Yoshio, T ;
Takeda, A ;
Masuyama, JI ;
Mimori, A ;
Kano, S ;
Minota, S .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 82 (02) :141-148