Savón C, Laferté J, Goyenechea A, Valdivia A, Morier L, Tejeiro Y
Instituto de Medicina Tropical Pedro Kourí.
Rev Cubana Med Trop. 1996;48(3):161-2.
An ultramicro ELISA assay of double antibody for the detection of IgG antibodies to the respiratory syncytial virus (RSV) was standardized. It was used a RVS antiprotein F monoclonal antibody produced by the Genetic Engineering and Biotechnology Center (GEBC) in Havana. The use of this antibody allowed to include crude antigenic preparations instead of purified fractions, which caused a significant reduction of the reactivity obtained with the antigen control. The assay conditions were determined by crossed titration. It was obtained a sensitivity of 97.2%, a coincidence of 91%, and a specificity of 83.3% of the UMELISA as regards the complement fixation. The results may be qualitatively expressed or by antibody titres using only one serum dilution (1:40) and a pattern curve.
一种用于检测呼吸道合胞病毒(RSV)IgG抗体的双抗体超微量ELISA检测方法得到了标准化。使用的是哈瓦那基因工程和生物技术中心(GEBC)生产的RVS抗蛋白F单克隆抗体。该抗体的使用使得可以采用粗制抗原制剂而非纯化组分,这导致与抗原对照相比所获得的反应性显著降低。检测条件通过交叉滴定来确定。就补体结合试验而言,超微量ELISA的灵敏度为97.2%,符合率为91%,特异性为83.3%。结果可以仅使用一种血清稀释度(1:40)并通过模式曲线进行定性表达或抗体滴度表示。