Mikkelsen Heidi, Aagaard Claus, Nielsen Søren Saxmose, Jungersen Gregers
National Veterinary Institute, Technical University of Denmark, Bülowsvej 27, 1790 Copenhagen V, Denmark.
Vet Immunol Immunopathol. 2012 Jun 15;147(1-2):69-76. doi: 10.1016/j.vetimm.2012.04.002. Epub 2012 Apr 17.
Paratuberculosis is a chronic infection of the intestine of ruminants caused by Mycobacterium avium subsp. paratuberculosis (MAP). Early stage MAP infection can be detected by measuring cell-mediated immune responses using the interferon gamma (IFN-γ) assay. Whole blood samples are cultured overnight with specific MAP antigens followed by quantification of IFN-γ by ELISA. It is recommended that the time interval from sampling to culture does not exceed eight hours but addition of the co-stimulating cytokine interleukin 12 (IL-12) or anti-IL-10 antibodies to culture have been demonstrated to enhance IFN-γ responses of cultures stimulated with Johnin purified protein derivative (PPDj). Here we examined the correlation of IFN-γ production in response to PPDj and 15 recombinant antigens in day-old blood samples from heifers 10-21 months of age from a MAP infected herd with addition of either recombinant bovine IL-12 or anti-bovine IL-10 antibody with IFN-γ production in sample day samples. IFN-γ responses of sample day samples showed high correlation with responses to some antigens in day-old samples with addition of IL-12 or anti-IL-10 antibodies to cultures, indicating that day-old protocols can be applied as an alternative to the conventional IFN-γ protocol. Immunogenicity of the novel antigens was generally low for day-old samples. The most promising antigen using the day-old protocol with addition of IL-12 was latency protein LATP-2 as correlations, immunogenicity and diagnostic specificity collectively was high. The latency protein LATP-1 was the most promising antigen in the day-old protocol with addition of anti-IL-10 antibodies.
副结核病是由鸟分枝杆菌副结核亚种(MAP)引起的反刍动物肠道慢性感染。早期MAP感染可通过使用干扰素γ(IFN-γ)检测法测量细胞介导的免疫反应来检测。全血样本与特定的MAP抗原一起培养过夜,然后通过ELISA对IFN-γ进行定量。建议从采样到培养的时间间隔不超过8小时,但已证明在培养中添加共刺激细胞因子白细胞介素12(IL-12)或抗IL-10抗体可增强用副结核菌素纯化蛋白衍生物(PPDj)刺激的培养物的IFN-γ反应。在此,我们检测了来自感染MAP牛群的10至21月龄小母牛日龄血液样本中,添加重组牛IL-12或抗牛IL-10抗体后,对PPDj和15种重组抗原产生的IFN-γ与样本日样本中IFN-γ产生之间的相关性。样本日样本的IFN-γ反应与添加IL-12或抗IL-10抗体到培养物中的日龄样本对某些抗原的反应高度相关,这表明日龄检测方案可作为传统IFN-γ检测方案的替代方法。对于日龄样本,新型抗原的免疫原性普遍较低。在添加IL-12的日龄检测方案中,最有前景的抗原是潜伏蛋白LATP-2,因为其相关性、免疫原性和诊断特异性总体较高。在添加抗IL-10抗体的日龄检测方案中,潜伏蛋白LATP-1是最有前景的抗原。