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免疫比浊法检测可溶性免疫复合物:方法学与临床应用

Nephelometric detection of soluble immune complexes: methodology and clinical applications.

作者信息

Virella G, Hipp W A, John J F, Kahaleh B, Ford M, Fudenberg H H

出版信息

Int Arch Allergy Appl Immunol. 1979;58(4):402-10. doi: 10.1159/000232219.

Abstract

We have developed a method for the detection of immune complexes by laser nephelometry which is simple, reproducible, suitable for automation, and generally adaptable for diagnostic testing. Light dispersion by antigen-antibody complexes in the test samples is measured after addition of polymeric buffer, which enhances the aggregation of complexes but does not significantly affect unbound immunoglobulins. The method was used to measure immune complexes formed in vitro by incubation of tetanus toxoid with serum from a rabbit previously hyperimmunized with the same antigen, and to compare the levels of immune complexes in human sera obtained from normal adults and from 37 patients with collagen vascular diseases or endocarditis. When precautions were taken to avoid interference produced by the presence of lipoproteins or by freezing of the samples, the results obtained with human sera were consistent with those expected for normal controls and for patients with conditions thought to be associated with the presence of soluble immune complexes.

摘要

我们开发了一种通过激光散射比浊法检测免疫复合物的方法,该方法简单、可重复、适用于自动化,并且一般适用于诊断检测。在加入聚合缓冲液后,测量测试样品中抗原-抗体复合物引起的光散射,聚合缓冲液可增强复合物的聚集,但对未结合的免疫球蛋白影响不大。该方法用于测量破伤风类毒素与先前用相同抗原高度免疫的兔血清在体外孵育形成的免疫复合物,并比较正常成年人以及37例胶原血管疾病或心内膜炎患者的人血清中免疫复合物的水平。当采取预防措施避免脂蛋白的存在或样品冷冻产生的干扰时,用人血清获得的结果与正常对照以及被认为与可溶性免疫复合物存在相关疾病患者的预期结果一致。

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