Fiscus S A, Mildbrand M M, Gordon J C, Teramoto Y A, Winston S
Am J Vet Res. 1985 Apr;46(4):859-63.
A rapid screening assay for determining antibodies to canine parvovirus in dog serum using monoclonal antibodies and enzyme-linked immunosorbent assay (ELISA) technology was developed. The ELISA could be read visually, and the results correlated well with serum neutralization (SN) and hemagglutination inhibition (HI) titers. Sera with SN less than or equal to 1:4 or HI less than or equal to 1:10 had an 87.9% correlation with ELISA and sera with SN greater than or equal to 1:64 or HI greater than or equal to 1:80 had a 94.4% correlation. The assay took only 10 to 15 minutes to perform and did not require specialized equipment. The ELISA should be useful in monitoring dogs for the presence of maternal antibodies against parvovirus and for determining seroconversion after vaccination.
利用单克隆抗体和酶联免疫吸附测定(ELISA)技术,开发了一种用于检测犬血清中犬细小病毒抗体的快速筛查检测方法。该ELISA检测可通过肉眼读取结果,其结果与血清中和(SN)及血凝抑制(HI)效价相关性良好。SN小于或等于1:4或HI小于或等于1:10的血清与ELISA的相关性为87.9%,而SN大于或等于1:64或HI大于或等于1:80的血清与ELISA的相关性为94.4%。该检测方法仅需10至15分钟即可完成,且无需专门设备。该ELISA检测在监测犬体内针对细小病毒的母源抗体以及确定疫苗接种后的血清转化情况方面应具有实用价值。