Lybeck Kari R, Storset Anne K, Olsen Ingrid
Department of Animal Health, National Veterinary Institute, Oslo, Norway.
Clin Vaccine Immunol. 2009 Jul;16(7):1003-11. doi: 10.1128/CVI.00114-09. Epub 2009 May 6.
The gamma interferon assay is used to identify Mycobacterium avium subsp. paratuberculosis-infected animals. It has been suggested that regulatory mechanisms could influence the sensitivity of the test when it is performed with cells from cattle and that the neutralization of interleukin-10 (IL-10) in vitro would increase the gamma interferon responses. To investigate the regulatory mechanisms affecting the gamma interferon assay with cells from goats, blood was collected from M. avium subsp. paratuberculosis-infected, M. avium subsp. paratuberculosis-exposed, and noninfected goats. Neutralization of IL-10 by a monoclonal antibody resulted in increased levels of gamma interferon production in M. avium subsp. paratuberculosis purified protein derivative (PPDj)-stimulated samples from both infected and exposed goats. However, the levels of gamma interferon release were also increased in unstimulated cells and in PPDj-stimulated cells from some noninfected animals following neutralization. Depletion of putative regulatory CD25(high) T cells had no clear effect on the number of gamma-interferon-producing cells. The IL-10-producing cells were identified to be mainly CD14(+) major histocompatibility complex class II-positive monocytes in both PPDj-stimulated and control cultures and not regulatory T cells. However, possible regulatory CD4(+) CD25(+) T cells produced IL-10 in response to concanavalin A stimulation. The numbers of CD4(+), CD8(+), and CD8(+) gammadelta T-cell receptor-positive cells producing gamma interferon increased following IL-10 neutralization. These results provide insight into the source and the role of IL-10 in gamma interferon assays with cells from goats and suggest that IL-10 from monocytes can regulate both innate and adaptive gamma interferon production from several cell types. Although IL-10 neutralization increased the sensitivity of the gamma interferon assay, the specificity of the test could be compromised.
γ干扰素检测用于鉴定感染副结核分枝杆菌的动物。有人提出,当用牛的细胞进行检测时,调节机制可能会影响检测的敏感性,并且体外中和白细胞介素10(IL-10)会增加γ干扰素反应。为了研究影响山羊细胞γ干扰素检测的调节机制,从感染副结核分枝杆菌、接触过副结核分枝杆菌和未感染的山羊采集血液。用单克隆抗体中和IL-10导致来自感染和接触过副结核分枝杆菌的山羊的纯化蛋白衍生物(PPDj)刺激样本中γ干扰素产生水平增加。然而,中和后,一些未感染动物的未刺激细胞和PPDj刺激细胞中的γ干扰素释放水平也增加了。去除假定的调节性CD25(高) T细胞对产生γ干扰素的细胞数量没有明显影响。在PPDj刺激的培养物和对照培养物中,产生IL-10的细胞主要被鉴定为CD14(+)主要组织相容性复合体II类阳性单核细胞,而非调节性T细胞。然而,可能的调节性CD4(+) CD25(+) T细胞在受到刀豆球蛋白A刺激时产生IL-10。中和IL-10后,产生γ干扰素的CD4(+)、CD8(+)和CD8(+) γδ T细胞受体阳性细胞数量增加。这些结果深入了解了IL-10在山羊细胞γ干扰素检测中的来源和作用,并表明单核细胞产生的IL-10可以调节几种细胞类型的先天性和适应性γ干扰素产生。虽然中和IL-10增加了γ干扰素检测的敏感性,但检测的特异性可能会受到影响。