PACE 和 CTB_ELISA 检测在诊断典型猪瘟 (CSF) 和相应疫苗质量控制中的价值{在}马达加斯加

Of MaminiainaFOFIFA-DRZVP, IMVAVET, M. KokoIMVAVET, J. J. RajaonarisonIMVAVET, R. RazafindrakotoIMVAVET, J. RavaomananaFOFIFA-DRZVP, A. D. Shannon
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引用次数: 0

摘要

从 1994 年起,我们开始使用 ELISA(酶联免疫吸附试验)诊断五氯苯酚。这是一种用于捕捉样本中可能含有的抗原(PACE)的酶联免疫吸附试验。这种检测方法的优势在于它完全不依赖于细胞培养。此外,它还具有快速的特点:在 36 小时内即可获得结果。在澳大利亚进行的一项标准化研究显示,该检测方法的灵敏度(Se)为 99%,特异度(Sp)接近 100%,阴性预测值(NPV)为 99.7%。捕获酶联免疫吸附试验的一种变体 CTB-ELISA 或复合捕获阻断酶联免疫吸附试验可测定动物血清中针对非结构蛋白 p80(或 NS3)的抗体数量。抗 NS3 抗体水平的评估可以很好地评估中和抗体的水平,因为这两种抗体(第一种通过 CTB-ELISA 获得,第二种通过血清中和(VNT)获得)之间的相关系数非常高(r = 0.98)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Valeur des tests PACE et CTB_ELISA dans le diagnostic de la peste porcine classique (PPC) et le contr{ô}le de qualit{é} du vaccin correspondant {à} Madagascar
From 1994, we began to use ELISA (Enzyme Linked Immunosorbent Assay) in the diagnosis of PCP. This is aELISA for capturing antigens (PACE) possibly contained in the samples. The advantage of this test comes from the fact that it is completelyindependent of cell cultures. In addition, it is fast: the result can be obtained in less than 36 hours. A study of its standardizationcarried out in Australia gave a sensitivity (Se) of 99%, a specificity (Sp) close to 100% and a negative predictive value (NPV) of 99.7%. Due to its high specificity, the test gives a negative result to all true negatives, in other words, the negatives of the test correspond to thetrue negatives. A variant of the capture ELISA, the CTB-ELISA or complex trapping blocking ELISA allows the quantity of antibodies to be measureddirected against the non-structural protein, p80 (or NS3), contained in animal sera. Evaluation of the level of anti-NS3 antibodiesconstitutes an excellent assessment of the level of neutralizing antibodies because the correlation coefficient between these two types of antibodies, the firstobtained by CTB-ELISA, and the second by serum neutralization (VNT), is very high (r = 0.98).The two tests being capable, one of detecting pestiviral antigens and the other of measuring antibodies specific to each of thegroups, constitutes an excellent tool for the qualitative control of anti-CSF vaccine.
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