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Detection of cross-reactive anti-DNA antibody idiotypes in the serum of systemic lupus erythematosus patients and of their relatives.

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TLDR
Two common cross-reacting anti-DNA antibody idiotypes designated 16/6 and 32/15, previously identified in the serum of patients who have systemic lupus erythematosus, were found in 147 first-degree relatives, implying that high-frequency germ-line genes exist among l upus relatives, as well as patients.
Abstract
Two common cross-reacting anti-DNA antibody idiotypes designated 16/6 and 32/15, previously identified in the serum of patients who have systemic lupus erythematosus, were found in 24% and 7%, respectively, of 147 first-degree relatives. These findings imply that high-frequency germ-line genes exist among lupus relatives, as well as patients. These dominant or public anti-DNA antibody idiotypes are not likely to be pathogenic factors, but are probably a genetically associated phenomenon.

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Systemic lupus erythematosus

TL;DR: Systemic lupus erythematosus is a relapsing and remitting disease, and treatment aims are threefold: managing acute periods of potentially life-threatening ill health, minimizing the risk of flares during periods of relative stability, and controlling the less life- threatening, but often incapacitating day to day symptoms.
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The mosaic of autoimmunity.

TL;DR: A brief review of immunobiology in order to arrive at a suitable definition of auto-immunity is given in this paper, followed by a concise description of the current theories regarding the development of autoimmune disease and the factors known to be associated with these illnesses.
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Polymorphism at the C-reactive protein locus influences gene expression and predisposes to systemic lupus erythematosus

TL;DR: The hypothesis that defective disposal of potentially immunogenic material is a contributory factor in lupus pathogenesis is supported and the identification of polymorphisms that determine basal CRP levels has implications in ischaemic heart disease, where CRP level is an important predictor of risk.
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Interleukin–1 receptor antagonist gene polymorphism as a disease severity factor in systemic lupus erythematosus

TL;DR: It is postulate that the association of this polymorphism with disease severity is a widespread feature of common inflammatory and autoimmune diseases.
References
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Journal ArticleDOI

The 1982 revised criteria for the classification of systemic lupus erythematosus

TL;DR: The 1971 preliminary criteria for the classification of systemic lupus erythematosus (SLE) were revised and updated to incorporate new immunologic knowledge and improve disease classification and showed gains in sensitivity and specificity.
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Polyspecific monoclonal lupus autoantibodies reactive with both polynucleotides and phospholipids

TL;DR: The polyspecific reactivity of a single molecular species of lupusAutoantibody suggests that some of the diverse serological abnormalities of SLE may be a result of the binding of certain autoantibodies to a phosphodiester-containing epitope that is present in diverse biological molecules.
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Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.

TL;DR: The known association of systemic lupus erythematosus with uncommon inherited and acquired deficiencies of complement components suggests, however, that the presence of null alleles for C4A and C4B, as well as C2, found in most of the patients, is relevant to their genetic susceptibility to this disease.
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Polyspecificity of Monoclonal Lupus Autoantibodies Produced by Human-Human Hybridomas

TL;DR: The findings suggest that DNA itself need not be the immunogenic stimulus for autoantibody formation in systemic lupus erythematosus, and may be explained by the presence of appropriately spaced phosphodiester groups in both the polynucleotides and the phospholipid.
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