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Fluorometric immunoassay for detection of anti-dsDNA antibodies

机译:荧光免疫法检测抗dsDNA抗体

摘要

The present invention relates to the field of immunological methods, more precisely to the field of detection methods for antibodies against double-stranded DNA (dsDNA) for diagnostics of chronic autoimmune diseases, such as systemic lupus erythematosus (SLE). The fluorometric immunoassay method for detection of anti-dsDNA solves the technical problem of designing a method for detection of the aforesaid antibodies, which would be faster, cheaper and less toxic as the standard Farr-RIA method, but would have the same diagnostic specificity (which is 100%) and improved diagnostic sensitivity (for 3%). Detection of anti-dsDNA is based on detection of fluorescence in two fractions of samples, in the supernatant and in the sample with a precipitate, which contains immune complexes composed of added dsDNA and anti-dsDNA present in the patient's serum, wherein the detected fluorescence is a consequence of binding fluorescent dyes with dsDNA bound in the complexes or with free dsDNA. The method according to the invention allows obtaining reliable results, fast sample analysis and results availability to the attending physician, use of human and environmentally safe chemicals and lowering of costs in comparison to the standard Farr-RIA method.
机译:本发明涉及免疫学方法领域,更确切地说,涉及用于诊断诸如系统性红斑狼疮(SLE)之类的慢性自身免疫疾病的双链DNA(dsDNA)抗体的检测方法领域。用于检测抗dsDNA的荧光免疫测定方法解决了设计用于检测上述抗体的方法的技术问题,该方法与标准Farr-RIA方法相比更快,更便宜且毒性更小,但诊断特异性相同( (100%)和更高的诊断灵敏度(3%)。抗dsDNA的检测是基于检测两部分样品中上清液和带有沉淀物的样品中的荧光,其中包含由患者血清中存在的dsDNA和抗dsDNA组成的免疫复合物,其中检测到的荧光这是荧光染料与复合物中结合的dsDNA或游离dsDNA结合的结果。与标准的Farr-RIA方法相比,根据本发明的方法允许获得可靠的结果,快速的样品分析和主治医生的结果可用性,人类和环境安全化学品的使用以及降低成本。

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