Nielsen C M, Hansen K, Andersen H M, Gerstoft J, Vestergaard B F
Enterovirus Department, Statens Seruminstitut, Copenhagen, Denmark.
J Virol Methods. 1987 Jun;16(3):195-208. doi: 10.1016/0166-0934(87)90004-8.
In this inhibition immunoassay undiluted serum reacts in solution with crude cellular CMV antigen in wells of microtestplates coated with hyperimmune CMV-reactive monkey IgG. CMV antibodies in the serum under test block (completely or partial) the fixation of antigen to the capture layer. Unblocked antigenic activity is in subsequent steps measured by the use of biotinylated CMV-reactive monkey IgG and peroxidase-conjugated avidin. The assay was evaluated in comparison with the CF test and was found superior both in terms of qualitative and quantitative detection of CMV antibodies. The results were uninfluenced by the presence in the sera of rheumatoid factor or autoantibodies (antinuclear antibodies). A characteristic feature of this inhibition immunoassay was the absence of equivocal results as demonstrated by analysis of 500 donor sera which were classified in two distinct separate groups: reactive and nonreactive. The assay is simple and reproducible and provides for a good reagent economy. Crude antigen can be used without sacrifice of specificity. Antigen from one Roux bottle proved sufficient for 25,000 duplicate tests.
在这种抑制免疫测定中,未稀释的血清在溶液中与包被有超免疫巨细胞病毒反应性猴IgG的微量滴定板孔中的粗细胞巨细胞病毒抗原发生反应。待测血清中的巨细胞病毒抗体阻断(完全或部分)抗原与捕获层的结合。在后续步骤中,通过使用生物素化的巨细胞病毒反应性猴IgG和过氧化物酶偶联的抗生物素蛋白来测量未被阻断的抗原活性。与补体结合试验相比,对该测定进行了评估,发现在巨细胞病毒抗体的定性和定量检测方面均更具优势。血清中类风湿因子或自身抗体(抗核抗体)的存在对结果没有影响。通过对500份供体血清进行分析,将其分为反应性和非反应性两个不同的单独组,结果表明这种抑制免疫测定的一个特征是没有模棱两可的结果。该测定简单且可重复,试剂经济性良好。可以使用粗抗原而不牺牲特异性。来自一个鲁氏瓶的抗原被证明足以进行25,000次重复试验。