Matsuo T, Nishi S, Hirai H, Osato T
Int J Cancer. 1976 Oct 15;18(4):453-7. doi: 10.1002/ijc.2910180409.
A useful method for the detection and assay of Epstein-Barr virus (EBV)-related soluble antigen has been developed by the application of the indirect single radial immunodiffusion technique which is frequently used for quantitative measurements of immunoglobulins and other soluble proteins. When the extracts of EBV-determined nuclear antigen (EBNA)-positive non-producer cells (Raji and NC-37) were applied to agar plates containing seropositive human serum, followed by overlay with anti-human IgG serum, ring-shaped precipitates with high specificity were clearly evident. The size of such precipitin rings was proportional to the amount of the antigen. This method is simple and applicable for a quantitative assay of a particular EBV-related soluble antigen and antibody and the sensitivity is equivalent to that seen with the complement fixation test.
通过应用间接单扩散免疫技术,已开发出一种检测和测定爱泼斯坦-巴尔病毒(EBV)相关可溶性抗原的有用方法,该技术常用于定量测量免疫球蛋白和其他可溶性蛋白质。当将EBV决定的核抗原(EBNA)阳性非产生细胞(Raji和NC-37)的提取物应用于含有血清阳性人血清的琼脂平板,然后覆盖抗人IgG血清时,具有高特异性的环形沉淀清晰可见。这种沉淀环的大小与抗原量成正比。该方法简单,适用于特定EBV相关可溶性抗原和抗体的定量测定,其灵敏度与补体结合试验相当。