CHANGES IN ANTIBODIES TO C1Q PREDICT RENAL RELAPSES IN SYSTEMIC LUPUS-ERYTHEMATOSUS

被引:149
作者
COREMANS, IEM
SPRONK, PE
BOOTSMA, H
DAHA, MR
VANDERVOORT, EAM
KATER, L
BREEDVELD, FC
KALLENBERG, CGM
机构
[1] UNIV LEIDEN HOSP,DEPT RHEUMATOL,2300 RC LEIDEN,NETHERLANDS
[2] UNIV LEIDEN HOSP,DEPT NEPHROL,2300 RC LEIDEN,NETHERLANDS
[3] UNIV GRONINGEN HOSP,DEPT CLIN IMMUNOL,9713 EZ GRONINGEN,NETHERLANDS
[4] UNIV UTRECHT HOSP,DEPT INTERNAL MED,UTRECHT,NETHERLANDS
关键词
ANTI-C1Q ANTIBODIES; ANTI-DOUBLE-STRANDED DNA ANTIBODIES; LUPUS NEPHRITIS;
D O I
10.1016/0272-6386(95)90595-2
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The presence of elevated plasma levels of autoantibodies against Clq, a subcomponent of the first component of complement in sera of patients with systemic lupus erythematosus (SLE) has been found to be associated with renal involvement, The purpose of this study was to determine whether increases in anti-Clq antibodies (anti-C1q) precede renal involvement in SLE, Forty-three SLE patients were studied longitudinally to determine the relationship between manifestations of the disease and levels of anti-Clq as well as to identify antibodies against double-stranded DNA (anti-dsDNA). Increased levels of anti-Clq were detected in all 14 of the patients who developed proliferative lupus nephritis out of 17 patients with renal relapses, which was significantly more frequent (P < 0.005) than in patients with nonrenal relapses (six of 16 patients) or with inactive disease (two of 10 patients). Increased anti-dsDNA levels were observed in 14 of 17 patients with renal relapses compared with 15 of 16 patients with nonrenal relapses and five of 10 patients with inactive disease, Significant increases in anti-Clq levels prior to the relapse occurred in 10 of 14 patients who developed proliferative nephritis and in three of 16 patients with nonrenal relapses, Significant increases in anti-dsDNA levels occurred in 11 patients of the former group and in nine patients of the latter group, No significant increases in anti-Clq or anti-dsDNA levels were observed in the patients with inactive disease, The mean time period between the occurrence of a significant increase in anti-Clq or anti-dsDNA level and the moment of renal relapse for both antibodies was 2.3 months, These results suggest that an increase in anti-Clq level has a predictive value for an ensuing renal relapse of proliferative lupus nephritis, and that serial measurements of anti-Clq levels might be useful in the management of SLE patients. (C) 1995 by the National Kidney Foundation, Inc.
引用
收藏
页码:595 / 601
页数:7
相关论文
共 35 条
[1]
ADLER MK, 1975, ANN RHEUM DIS, V34, P440
[2]
EVIDENCE FOR THE PRESENCE OF AUTOANTIBODIES TO THE COLLAGEN-LIKE PORTION OF C1Q IN SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ANTES, U ;
HEINZ, HP ;
LOOS, M .
ARTHRITIS AND RHEUMATISM, 1988, 31 (04) :457-464
[3]
ANTI-NATIVE DNA DETECTION BY THE CRITHIDIA-LUCILIAE METHOD - IMPROVED GUIDE TO THE DIAGNOSIS AND CLINICAL MANAGEMENT OF SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
BALLOU, SP ;
KUSHNER, I .
ARTHRITIS AND RHEUMATISM, 1979, 22 (04) :321-327
[4]
COREMANS IEM, 1992, CLIN EXP IMMUNOL, V87, P256
[5]
COREMANS IEM, 1992, IMMUNOBIOLOGY, V184, P417
[6]
CORRELATION BETWEEN LEVELS OF DNA ANTIBODIES AND CLINICAL DISEASE ACTIVITY IN SLE - RETROSPECTIVE EVALUATION [J].
DAVIS, P ;
PERCY, JS ;
RUSSELL, AS .
ANNALS OF THE RHEUMATIC DISEASES, 1977, 36 (02) :157-159
[7]
IMMUNOLOGICAL EVENTS PRECEDING CLINICAL EXACERBATION OF SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
EPSTEIN, WV .
AMERICAN JOURNAL OF MEDICINE, 1973, 54 (05) :631-636
[8]
ANTIBODIES TO COMPONENTS OF EXTRACTABLE NUCLEAR ANTIGEN [J].
FARBER, SJ ;
BOLE, GG .
ARCHIVES OF INTERNAL MEDICINE, 1976, 136 (04) :425-431
[9]
THE 1ST INTERNATIONAL STANDARD FOR ANTIBODIES TO DOUBLE-STRANDED DNA [J].
FELTKAMP, TEW ;
KIRKWOOD, TBL ;
MAINI, RN ;
AARDEN, LA .
ANNALS OF THE RHEUMATIC DISEASES, 1988, 47 (09) :740-746
[10]
ANTI-DNA ACTIVITY IN SYSTEMIC LUPUS ERYTHEMATOSUS - DIAGNOSTIC AND THERAPEUTIC GUIDE [J].
HUGHES, GRV ;
COHEN, SA ;
CHRISTIAN, CL .
ANNALS OF THE RHEUMATIC DISEASES, 1971, 30 (03) :259-+