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Assessment of a protein cocktail-based skin test for bovine tuberculosis in a double-blind field test in cattle

机译:评估牛在牛的双盲野外测试中基于蛋白质鸡尾酒的皮肤测试

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Bovine tuberculosis (bTB) is a worldwide zoonosis caused mainly by Mycobacterium bovis. The traditional diagnostic method used often is the tuberculin skin test, which uses bovine purified protein derivatives (PPD-B). However, it is difficult to maintain uniformity of PPD-B from batch to batch, and it shares common antigens with nonpathogenic environmental mycobacteria. To overcome these problems, M. bovis-specific antigens that showed good T cell stimulation, such as CFP-10, ESAT-6, Rv3615c, etc., have been used in the skin test, but there have been no large-scale clinical studies on these antigens. In this study, two combinations (CFP-10/ESAT-6/TB10.4 protein cocktail and CFP-10/ESAT-6/Rv3872/MPT63 protein cocktail) were developed and used as stimuli in the skin test. Cattle were double-blind tested to assess the efficiency of the protein cocktail-based skin tests. The results showed that the CFP-10/ESAT-6/TB10.4 protein cocktail-based skin test can differentiate TB-infected cattle from Mycobacterium avium-infected ones and that it shows a high degree of agreement with the traditional tuberculin skin test (k=0.8536) and gamma interferon (IFN-γ) release assay (k=0.8154). Compared to the tuberculin skin test, the relative sensitivity and relative specificity of the CFP-10/ESAT-6/TB10.4-based skin test were 87% and 97%, respectively., The relative sensitivity and relative specificity of the CFP-10/ESAT-6/TB10.4-based skin test were 93% and 92%, respectively, on comparison with the IFN-γ release assay. The correlation between the increases in skin thickness observed after the inoculation of stimuli was high (PPD-B versus CFP-10/ESAT-6/TB10.4, Spearman r of 0.8435). The correlation between the optical density at 450 nm (OD450) obtained after blood stimulation with PPD-B and the increase in skin thickness observed after inoculation of the CFP-10/ESAT-6/TB10.4 protein cocktail was high (Spearman r=0.7335). Therefore, the CFP-10/ESAT-6/TB10.4- based skin test responses correlate to traditional measures of bovine TB evaluation, including skin test and gamma interferon release assay.
机译:牛结核病(BTB)是主要由牛分枝杆菌引起的全球人畜共患病。通常使用的传统诊断方法是结核蛋白皮肤测试,该测试使用牛纯化的蛋白质衍生物(PPD-B)。但是,很难从批处理到批处理的PPD-B均匀性,并且与非致病性环境分枝杆菌共享共同的抗原。为了克服这些问题,在皮肤测试中使用了表现出良好T细胞刺激的Bovis特异性抗原,例如CFP-10,ESAT-6,RV3615C等这些抗原的研究。在这项研究中,开发了两种组合(CFP-10/ESAT-6/TB10.4蛋白鸡尾酒和CFP-10/ESAT-6/RV3872/MPT63蛋白鸡尾酒),并用作皮肤测试中的刺激。对牛进行双盲测试,以评估基于蛋白质鸡尾酒的皮肤测试的效率。结果表明,基于蛋白质鸡尾酒的皮肤测试CFP-10/ESAT-6/TB10.4可以将感染的TB感染的牛与鸟分枝杆菌感染的牛区分开,并且与传统的结核蛋白皮肤测试显示高度一致( k = 0.8536)和伽马干扰素(IFN-γ)释放分析(k = 0.8154)。与结核蛋白皮肤测试相比,基于CFP-10/ESAT-6/TB10.4的相对灵敏度和相对特异性分别为87%和97%。与IFN-γ释放测定法相比,基于10/ESAT-6/TB10.4的皮肤测试分别为93%和92%。接种刺激后观察到的皮肤厚度的增加之间的相关性很高(PPD-B与CFP-10/ESAT-6/TB10.4,Spearman R为0.8435)。血液刺激后450 nm(OD450)的光密度与PPD-B获得的相关性与接种CFP-10/ESAT-6/TB10.4蛋白质鸡尾酒后观察到的皮肤厚度增加(Spearman r = Spearman r =) 0.7335)。因此,基于CFP-10/ESAT-6/TB10.4的皮肤测试反应与牛TB评估的传统措施相关,包括皮肤测试和伽马干扰素释放分析。

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