Yang D P, Goldberg K M, Ma X D, Magargle W, Rappaport R
Wyeth Ayerst Research, Philadelphia, Pennsylvania 19101, USA.
Clin Diagn Lab Immunol. 1998 Nov;5(6):780-3. doi: 10.1128/CDLI.5.6.780-783.1998.
A fluorescent focus identification assay (FFIDA) was developed for use in experimental studies and for quantitation of the components in a tetravalent live oral rotavirus vaccine. The assay utilizes four serotype-specific neutralizing monoclonal antibodies (MAb) to detect and quantify individual rotaviruses by immunofluorescence staining of fixed virus-infected monkey kidney cells. In mixed virus infections, all four MAb, W1 (serotype 1), 1C10 (serotype 2), R1 (serotype 3), and S4 (serotype 4), specifically stain the relevant homologous serotype without exhibiting any cross-reactivity against the other serotypes. Furthermore, the test is sensitive enough to differentiate at least twofold (0.3 log) differences in virus titer. The results of testing four individual experimental vaccine lots three or more consecutive times showed that all four lots contained similar proportions of the four vaccine strains as detected by the classical plaque neutralization identification test. The rapidity and efficiency of the FFIDA are desirable attributes that make it suitable for use in studies requiring identification and quantitation of one or more of the four major rotavirus serotypes.
开发了一种荧光灶鉴定试验(FFIDA),用于实验研究以及四价口服轮状病毒活疫苗成分的定量分析。该试验利用四种血清型特异性中和单克隆抗体(MAb),通过对固定的病毒感染猴肾细胞进行免疫荧光染色来检测和定量单个轮状病毒。在混合病毒感染中,所有四种单克隆抗体,即W1(血清型1)、1C10(血清型2)、R1(血清型3)和S4(血清型4),能特异性地对相关同源血清型进行染色,而不会对其他血清型表现出任何交叉反应。此外,该试验灵敏度足以区分病毒滴度至少两倍(0.3对数)的差异。对四个单独的实验疫苗批次连续三次或更多次进行检测的结果表明,通过经典蚀斑中和鉴定试验检测,所有四个批次所含四种疫苗株的比例相似。FFIDA的快速性和高效性是理想的特性,使其适用于需要鉴定和定量四种主要轮状病毒血清型中一种或多种血清型的研究。