Balsari A, Poli G, Molina V, Dovis M, Petruzzelli E, Boniolo A, Rolleri E
J Clin Pathol. 1980 Jul;33(7):640-3. doi: 10.1136/jcp.33.7.640.
An ELISA method was developed for the measurement of toxoplasma IgG antibodies in human serum using antigen-coated polystyrene beads as a solid phase and anti human IgG-horse radish peroxidase conjugate as an enzymatic tracer. In order to assess ELISA sensitivity and specificity, a between methods comparison was made using 'conventional' serological tests as reference (dye-test, crossover-linked immunoassay, passive haemagglutination, indirect immunofluorescence). From an analysis of the group classifications obtained some considerations emerged: the ELISA specificity looks comparable with that of the 'reference' tests, as no sample classified as negative by all these tests was ELISA-positive, and vice versa; ELISA appears to correlate better with haemagglutination and immunofluorescence, on the basis of the respective class frequencies; in particular, the number of positives, which is much lower for the dye-test and crossover-linked immunoassay, suggests that a higher sensitivity is reached in the former cases.
开发了一种酶联免疫吸附测定(ELISA)方法,以包被抗原的聚苯乙烯珠作为固相,抗人IgG-辣根过氧化物酶结合物作为酶标记物,用于检测人血清中的弓形虫IgG抗体。为了评估ELISA的敏感性和特异性,以“传统”血清学检测作为参考(染色试验、交叉连接免疫测定、被动血凝试验、间接免疫荧光法)进行了方法间比较。通过对所得组分类的分析得出了一些结论:ELISA的特异性看起来与“参考”试验相当,因为所有这些试验分类为阴性的样本没有一个在ELISA中呈阳性,反之亦然;基于各自的类别频率,ELISA似乎与血凝试验和免疫荧光法的相关性更好;特别是,染色试验和交叉连接免疫测定的阳性数要低得多,这表明在前一种情况下达到了更高的敏感性。