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首页> 外文期刊>Journal of Clinical Microbiology >Detection of serotype-specific antibodies or capsular antigen of Actinobacillus pleuropneumoniae by a double-label radioimmunoassay.
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Detection of serotype-specific antibodies or capsular antigen of Actinobacillus pleuropneumoniae by a double-label radioimmunoassay.

机译:通过双标记放射免疫分析法检测胸膜肺炎放线杆菌血清型特异性抗体或荚膜抗原。

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Diagnostic tests for Actinobacillus pleuropneumoniae have been problematic because current tests do not use a purified antigen and in most cases measure either antibody or antigen, but not both. We describe a Farr-type double-label radioimmunoassay that utilizes purified, serotype-specific, 3H-capsule to measure antibody to capsule directly or that can measure capsule in a sample indirectly by inhibition of antibody binding. The assay could detect about 1 ng of serotype-specific antibody in serum or at least 100 pg of capsule in a sample. Due to the sensitivity of the assay, false-positive results were common with neat sera (probably due to cross-reacting antibodies to unrelated antigens), but the specificity was improved when the sera were diluted 1:100. The radioimmunoassay should prove to be a useful reference method for research and diagnostic testing and for comparison of new assays for detection of capsule or antibodies to capsule.
机译:胸膜肺炎放线杆菌的诊断测试存在问题,因为当前的测试不使用纯化的抗原,并且在大多数情况下只能测量抗体或抗原,但不能同时测量两者。我们描述了一种Farr型双标记放射免疫测定法,它利用纯化的,血清型特异性的3H胶囊直接测量针对胶囊的抗体,或者可以通过抑制抗体结合来间接测量样品中的胶囊。该测定法可检测血清中约1 ng血清型特异性抗体或样品中至少100 pg胶囊。由于测定的敏感性,纯血清的假阳性结果很常见(可能是由于针对无关抗原的交叉反应抗体),但是当血清以1:100稀释时,特异性得到了改善。放射免疫测定法应被证明是用于研究和诊断测试以及比较用于检测胶囊或胶囊抗体的新方法的有用参考方法。

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