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提高猪布鲁氏菌病免疫诊断的特异性。

Improving the specificity of immunodiagnosis for porcine brucellosis.

作者信息

Thirlwall R E, Commander N J, Brew S D, Cutler S J, McGiven J A, Stack J A

机构信息

Department of Statutory and Exotic Bacteria, Veterinary Laboratories Agency, Addlestone, Weybridge, Surrey KT15 3NB, UK.

出版信息

Vet Res Commun. 2008 Mar;32(3):209-13. doi: 10.1007/s11259-007-9023-9. Epub 2007 Oct 13.

Abstract

This report describes the use of cell mediated immunity to improve specificity of current diagnosis for Brucella suis. Diagnosis is problematic due to cross reactions that lead to false positive serological reactions (FPSR) in the standard diagnostic tests. A common cause of this cross reactivity is infection with the organism Yersinia enterocolitica O:9. Gottingen mini-pigs were experimentally infected with B. suis biovar I field strain or Y. enterocolitica serotype O:9 biotype 3. Infection was followed for 70 days. During this time whole blood stimulation assays were set up using Brucella specific antigen. IFNgamma was measured in the supernatants (SN) from these assays by ELISA. Concurrent standard serological tests were carried out. The results indicate that the IFNgamma assay is specifically able to distinguish Y. enterocolitica O:9 infection from a B. suis infection in experimentally infected mini-pigs. These results represent an improvement in diagnostic specificity compared to currently used serological tests. Thus suggesting that in a surveillance setting this test could be applied as a confirmatory test in the face of FPSR.

摘要

本报告描述了利用细胞介导免疫来提高当前猪布鲁氏菌诊断特异性的方法。由于交叉反应会导致标准诊断测试中出现假阳性血清学反应(FPSR),因此诊断存在问题。这种交叉反应的一个常见原因是感染小肠结肠炎耶尔森氏菌O:9。用猪布鲁氏菌生物变种I田间菌株或小肠结肠炎耶尔森氏菌血清型O:9生物型3对哥廷根小型猪进行实验性感染。感染持续70天。在此期间,使用布鲁氏菌特异性抗原建立全血刺激试验。通过ELISA法测定这些试验上清液(SN)中的IFNγ。同时进行标准血清学检测。结果表明,IFNγ检测能够特异性地区分实验感染小型猪中O:9小肠结肠炎耶尔森氏菌感染和猪布鲁氏菌感染。与目前使用的血清学检测相比,这些结果代表了诊断特异性的提高。因此表明,在监测环境中,面对FPSR时,该检测可作为一种确证检测应用。

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