Coyle P K, Banks N, Schutzer S E
J Immunol Methods. 1984 Nov 16;74(1):191-7. doi: 10.1016/0022-1759(84)90380-6.
The Raji cell assay to detect immune complexes has been modified to a microtiter ELISA system. Raji cells were fixed to microplate wells, then reacted with serum samples or aggregated human IgG. Horseradish peroxidase-conjugated anti-human IgG was used to detect bound complexes. There was a linear relationship between aggregated IgG added and optical density reading, with less than 2 micrograms/ml of aggregated IgG readily detected. When applied to human serum this technique gave results comparable to those obtained with the standard Raji cell assay. The Raji micro-ELISA is simpler to perform than the standard assay, is equally reliable, and avoids the hazards of radioactivity.
用于检测免疫复合物的Raji细胞试验已被改进为一种微量滴定酶联免疫吸附测定(ELISA)系统。将Raji细胞固定在微孔板孔中,然后与血清样本或聚合人IgG反应。用辣根过氧化物酶偶联的抗人IgG来检测结合的复合物。加入的聚合IgG与光密度读数之间存在线性关系,易于检测到低于2微克/毫升的聚合IgG。当应用于人体血清时,该技术所得到的结果与标准Raji细胞试验所得到的结果相当。Raji微量ELISA比标准试验操作更简单,同样可靠,并且避免了放射性危害。