Department of Virology, Bernhard-Nocht-Institute for Tropical Medicine, Bernhard-Nocht-Str.74, 20359 Hamburg, Germany.
Med Microbiol Immunol. 2011 Nov;200(4):233-9. doi: 10.1007/s00430-011-0195-0. Epub 2011 May 1.
Immune complex (IC) ELISAs for IgG antibodies to various virus antigens have turned out to be both highly specific and sensitive. During incubation of a labelled antigen with the serum samples, ICs are formed, which bind to microtiter plates coated with rheumatoid factor (RF) IgM. Here, we describe an improved coating of the solid-phase support comparing various Fc-receptor molecules. IC ELISAs were applied to detect human IgG antibodies to the highly virus-specific ED3 domain of West Nile- and tick-borne encephalitis virus envelopes. Compared with other Fc-receptor molecules like RF or C1q, FcγRIIA (CD32) turned out to bind the ICs composed of IgG antibodies and peroxidase-labelled ED3 antigens more efficiently. Due to low background reactions, sera could be tested at a dilution of 1:10. Moreover, using CD32 instead of RF coating, anti-flavivirus antibodies could be detected in various animal species.
免疫复合物(IC)ELISA 法可用于检测针对各种病毒抗原的 IgG 抗体,该方法具有高特异性和高灵敏度。在标记抗原与血清样本孵育过程中,会形成免疫复合物,这些复合物可与类风湿因子(RF)IgM 包被的微孔板结合。在此,我们描述了一种改进的固相载体包被方法,比较了各种 Fc 受体分子。我们应用 IC ELISA 法检测针对西尼罗河病毒和蜱传脑炎病毒包膜高度特异性 ED3 结构域的人 IgG 抗体。与其他 Fc 受体分子如 RF 或 C1q 相比,FcγRIIA(CD32)更有效地结合由 IgG 抗体和过氧化物酶标记的 ED3 抗原组成的 IC。由于背景反应低,血清可以以 1:10 的稀释度进行检测。此外,使用 CD32 代替 RF 包被,可在各种动物物种中检测到抗黄病毒抗体。