Nomura M, Imai M, Takahashi K, Kumakura T, Tachibana K, Aoyagi S, Usuda S, Nakamura T, Miyakawa Y, Mayumi M
J Immunol Methods. 1983 Mar 25;58(3):293-300. doi: 10.1016/0022-1759(83)90357-5.
Utilizing monoclonal antibodies against human alpha-fetoprotein, 3 distinct antigenic determinants were identified. These antigenic determinants, provisionally designated a, b and c, were arranged in such a manner that the binding of one determinant with the corresponding antibody did not inhibit, or only barely inhibited the binding of antibodies directed to the other 2 determinants. Monoclonal antibodies with 3 different specificities were, therefore, applied to develop a sandwich-type solid-phase radioimmunoassay of the antigen in which wells were coated with anti-a, and radiolabeled anti-b together with radiolabeled anti-c was employed to detect the bound antigen. The 3-site sandwich radioimmunoassay involving 3 different determinants gave a higher sensitivity than 2-site assays in which only anti-b or anti-c was employed as a radiolabeled reagent, because the radioactivity of the 2 labeled antibodies was added on the antigen bound to immobilized anti-a.
利用抗人甲胎蛋白的单克隆抗体,鉴定出3种不同的抗原决定簇。这些抗原决定簇暂定为a、b和c,它们的排列方式是,一个决定簇与相应抗体的结合不会抑制,或仅轻微抑制针对其他两个决定簇的抗体的结合。因此,应用具有3种不同特异性的单克隆抗体开发了一种夹心型固相放射免疫分析法来检测该抗原,其中孔用抗a包被,并用放射性标记的抗b和放射性标记的抗c一起检测结合的抗原。涉及3种不同决定簇的3位点夹心放射免疫分析法比仅使用抗b或抗c作为放射性标记试剂的2位点分析法具有更高的灵敏度,因为两种标记抗体的放射性加在了与固定化抗a结合的抗原上。