ANTIBODIES TO DNA IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS - THEIR ROLE IN THE DIAGNOSIS, THE FOLLOW-UP AND THE PATHOGENESIS OF THE DISEASE

被引:25
作者
SMEENK, R
BRINKMAN, K
VANDENBRINK, H
TERMAAT, RM
BERDEN, J
NOSSENT, H
SWAAK, T
机构
[1] Central Laboratory of the Netherlands Red Cross Blood Transfusion Service and Laboratory for, and Clinical Immunology, University of Amsterdam
[2] Department of Nephrology, University Hospital, University of Nijmegen
[3] Department of Rheumatology, Dr Daniel Den Hoed Clinic, Rotterdam
关键词
Anti-DNA; Crithidia Luciliae; Crossreactivity; Diagnosis; ELISA; Farr Assay; Longitudinal study; Pathogenesis; PEG Assay; RIA; SLE;
D O I
10.1007/BF02205557
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this paper an overview of the present knowledge on antibodies against DNA will be presented. Diagnostic, prognostic and pathogenic aspects of anti-DNA will be highlighted. Detection of antibodies to DNA in the circulation of a patient by an assay selective for high avidity anti-DNA is highly diagnostic for SLE. Anti-DNA of low avidity occurs in rheumatic diseases other than SLE as well, making detection of such antibodies of less diagnostic value. Furthermore, data will be presented that show that the anti-DNA ELISA in its present form is not suited as a diagnostic tool. Not only disease features of SLE vary from patient to patient, anti-DNA avidity does so too. A relationship between anti-DNA avidity and clinical features can be found: high avidity anti-DNA is more abundant in patients with nephritis, low avidity anti-DNA in patients with CNS involvement. Prognostically, a steady increase of the level of high avidity anti-DNA generally heralds an upcoming exacerbation in a patient. Furthermore, 85% of the patients who do not have SLE at the time (high avidity) anti-DNA is detected in their serum, will develop the disease within the next few years. It is noteworthy, that patients with only low avidity anti-DNA in their circulation develop a more mild form of SLE; the (low) avidity of their anti-DNA seldomly increases during the course of their disease. The relevance of anti-DNA to the pathogenesis of SLE still is a matter of debate. On the one hand, the association of parameters of anti-DNA that determine the size of the complexes formed with DNA is in favour of the classical hypothesis, which states that SLE is primarily an immune complex disease. On the other hand, recent data on crossreactions of anti-DNA with phospholipids, glycosaminoglycans and other (polynegative) structures plead for a role of such crossreactivities in the pathogenesis of SLE. © 1990 Springer-Verlag.
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页码:100 / 110
页数:11
相关论文
共 49 条
[1]  
Hughes G.R.V., Connective tissue diseases, pp. 3-65, (1977)
[2]  
Lahita R.G., Systemic Lupus Erythematosus, pp. 1-1000, (1987)
[3]  
Stollar B.D., Nucleic acid antigens, The antigens, vol. I, pp. 1-85, (1973)
[4]  
Smeenk R.J.T., Westgeest A.A.A., Swaak A.J.G., Antinuclear antibody determination: the present state of diagnostic and clinical relevance, Scand J Rheumatol, 56, pp. 78-92, (1985)
[5]  
Roder J.C., Bell D.A., Singhal S.K., Regulation of the autoimmune plaqueforming cell response to singlestranded DNA (ssDNA) in vitro, J Immunol, 121, pp. 38-45, (1978)
[6]  
Fournie G.J., Lambert P.H., Miescher P.A., Release of DNA in the circulating blood and induction of anti-DNA antibodies after injection of bacterial lipopolysaccharides, Journal of Experimental Medicine, 140, pp. 1189-1196, (1974)
[7]  
Izui S., Zaldivar N.M., Scher I., Lambert P.H., Mechanism for the induction of anti-DNA antibodies by bacterial lipopolysaccharides in mice. I. Anti-DNA induction by LPS without significant release of DNA in the circulating blood, J Immunol, 119, pp. 2151-2157, (1977)
[8]  
Dighiero G., Lymberi P., Guilbert B., Ternynck T., Avrameas S., Natural autoantibodies constitute a substantial part of normal circulating immunoglobulins, Ann NY Acad Sci, 475, pp. 135-145, (1986)
[9]  
Ternynck T., Avrameas S., Murine natural monoclonal autoantibodies: a study of their polyspecificity and their affinities, Immunol Rev, 94, pp. 99-112, (1986)
[10]  
Cairns E., Block J., Bell D.A., Anti-DNA autoantibody producing hybridomas of normal human lymphoid cell origin, J Clin Invest, 74, pp. 880-889, (1984)