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Evaluation of cell mediated immune diagnostic tests to detect Mycobacterium avium subspecies paratuberculosis

机译:评估细胞介导的免疫诊断测试以检测鸟分枝杆菌亚种副结核病

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摘要

Mycobacterium avium subspecies paratuberculosis (MAP) causes Johne\u27s disease, a chronic progressive fatal disease of ruminants. Similar to tuberculosis, diagnostic tests based on detecting the organism or antibodies are not capable of detecting infected animals in the early stages. Consequently, diagnostic tests based upon the cell mediated immune response, such as the skin test and gamma interferon enzyme-linked immuno absorbent assay (ELISA), which have been successful at detecting tuberculosis need to be investigated further for paratuberculosis. The first paper evaluated the skin test in sheep along with two antibody based diagnostic tests using Bayesian statistical methods that estimate the sensitivity and specificity of diagnostic tests in multiple populations without a gold standard. The second paper used receiver operating characteristic (ROC) analysis to evaluate the accuracy of the gamma interferon (IFN-gamma) ELISA in subclinically infected sheep. These 2 studies similarly concluded the skin test and IFN-gamma ELISA had an estimated sensitivity of around 70% and a specificity of 98%. The next paper evaluated the environmental parameters necessary for handling whole blood for the IFN-gamma ELISA and assessed the validity of positive controls. The conclusion was blood should be maintained at room temperature, stimulated within 8 hours and phytohemaglutinin A (PHA) was the most accurate positive control tested in cattle. Finally the last paper attempts to further characterize the meaning of a positive response to the skin test or the IFN-gamma ELISA by assessing the consequences of environmental exposure to dead MAP. This study found that inhaled or ingested dead MAP does not stimulate a detectable response on the skin test or IFN-gamma ELISA.
机译:鸟分枝杆菌亚种副结核病(MAP)引起约翰尼氏病,这是一种反刍动物的慢性进行性致命疾病。与结核病类似,基于检测生物或抗体的诊断测试无法在早期检测出感染的动物。因此,已经成功地检测到结核病的基于细胞介导的免疫反应的诊断试验,例如皮肤试验和γ-干扰素酶联免疫吸附测定(ELISA),需要进一步研究。第一篇论文使用贝叶斯统计方法评估了绵羊的皮肤测试以及两种基于抗体的诊断测试,这些贝叶斯统计方法估计了在没有金标准的多个人群中诊断测试的敏感性和特异性。第二篇论文使用接收器工作特征(ROC)分析来评估亚临床感染的绵羊中γ干扰素(IFN-γ)ELISA的准确性。这两项研究类似地得出结论,皮肤测试和IFN-γELISA的估计灵敏度约为70%,特异性为98%。下一篇论文评估了用于IFN-γELISA的全血处理所必需的环境参数,并评估了阳性对照的有效性。结论是血液应保持在室温下,应在8小时内刺激,而植物血凝素A(PHA)是在牛中测试的最准确的阳性对照。最后,最后一篇论文试图通过评估暴露于死MAP的环境后果来进一步表征对皮肤测试或IFN-γELISA阳性反应的意义。这项研究发现,吸入或摄入的死亡MAP不会刺激皮肤试验或IFN-γELISA的可检测反应。

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    Robbe-Austerman, Suelee;

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  • 年度 2007
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