Oh Jin-Sik, Ha Gun-Woo, Cho Young-Shik, Kim Min-Jae, An Dong-Jun, Hwang Kyu-Kye, Lim Yoon-Kyu, Park Bong-Kyun, Kang BoKyu, Song Dae-Sub
Animal Genetics, Inc., Suwon, Kyunggi-do 440-290, Korea.
Clin Vaccine Immunol. 2006 Apr;13(4):520-4. doi: 10.1128/CVI.13.4.520-524.2006.
This study was performed to determine the feasibility of using whole serum to detect antibodies to canine parvovirus (CPV) under nonlaboratory conditions and to evaluate the performance characteristics of an immunochromatography assay kit. Precise detection of levels of antibody against CPV in puppies can be used to determine a vaccination schedule, because maternal antibodies frequently result in the failure of protective vaccination, and can also be used to determine the antibody levels of infected puppies. Several methods for the titration of CPV antibodies have been reported, including the hemagglutination inhibition (HI) assay, which is considered the "gold standard." These methods, however, require intricate and time-consuming procedures. In this study, a total of 386 serum specimens were tested. Compared to the HI assay, the rapid assay had a 97.1% sensitivity and a 76.6% specificity (with a cutoff HI titer of 1:80). This single-step assay could be performed rapidly and easily without special equipment. The kit provides a reliable method for detection of anti-CPV antibody where laboratory support and personnel are limited.
本研究旨在确定在非实验室条件下使用全血清检测犬细小病毒(CPV)抗体的可行性,并评估免疫层析检测试剂盒的性能特征。精确检测幼犬体内抗CPV抗体水平可用于确定疫苗接种计划,因为母源抗体常常导致保护性疫苗接种失败,还可用于确定感染幼犬的抗体水平。已有多种检测CPV抗体滴度的方法被报道,包括被视为“金标准”的血凝抑制(HI)试验。然而,这些方法需要复杂且耗时的操作步骤。在本研究中,共检测了386份血清样本。与HI试验相比,该快速检测方法的灵敏度为97.1%,特异性为76.6%(HI滴度截断值为1:80)。这种单步检测方法无需特殊设备即可快速、简便地进行。该试剂盒为在实验室支持和人员有限的情况下检测抗CPV抗体提供了一种可靠的方法。