Leinikki P O, Shekarchi I, Dorsett P, Sever J L
J Clin Microbiol. 1978 Oct;8(4):419-23. doi: 10.1128/jcm.8.4.419-423.1978.
A "microgram assay" is described in which solid-phase enzyme-linked immunosorbent assay is used for the determination of specific rubella immunoglobulin G (IgG) antibody levels in micrograms per milliliter of serum. The quantitation was based on a standard curve obtained by using a reference serum, for which the specific IgG content was assayed by immunochemical purification. IgG was first purified and specific rubella antibodies were separated by an immunoadsorbent prepared by linking rubella virus antigens to Sepharose 4B. By using IgG-specific conjugate, the levels of specific rubella IgG antibodies could then be determined from clinical samples. Seronegative samples showed antibody levels less than 1 microgram/ml, whereas levels up to several hundred micrograms per milliliter were detected in some postinfection sera. The correlation between microgram antibody levels and hemagglutination inhibition titers was linear. The method offers a simple and sensitive antibody assay which could be used both for the laboratory diagnosis of acute rubella and for the evaluation of immunity.
本文描述了一种“微克检测法”,该方法采用固相酶联免疫吸附测定法来测定血清中每毫升微克数的特异性风疹免疫球蛋白G(IgG)抗体水平。定量基于使用参考血清获得的标准曲线,该参考血清的特异性IgG含量通过免疫化学纯化进行测定。首先纯化IgG,然后通过将风疹病毒抗原与琼脂糖4B连接制备的免疫吸附剂分离特异性风疹抗体。通过使用IgG特异性结合物,随后可以从临床样本中测定特异性风疹IgG抗体水平。血清阴性样本的抗体水平低于1微克/毫升,而在一些感染后血清中检测到的水平高达数百微克/毫升。微克抗体水平与血凝抑制效价之间的相关性呈线性。该方法提供了一种简单且灵敏的抗体检测方法,可用于急性风疹的实验室诊断和免疫评估。