de Silva Kumudika, Begg Douglas, Whittington Richard
Faculty of Veterinary Science, The University of Sydney, Camden, NSW, Australia.
Vet Immunol Immunopathol. 2011 Jan;139(1):10-6. doi: 10.1016/j.vetimm.2010.07.022. Epub 2010 Aug 7.
Johne's disease is an enteric mycobacterial infection of ruminants that has significant global economic impact. The classic host reaction is one of an early T-cell mediate immune response, with predominant interferon gamma (IFNγ) activity; there is subsequent lowering of this response as animals reach the terminal stages of disease. Interleukin (IL)-10, which can suppress Th1-type and enhance Th2-type cytokine production, is considered to play a role in the later stages of Johne's disease. To determine the role of IL-10 throughout the course of Johne's disease we studied groups of sheep with either no Johne's disease (n=10), natural infection (n=30) or experimental infection (n=58). Disease status of the animals was comprehensively assessed by culture of Mycobacterium avium subsp. paratuberculosis (Mptb), histopathology and serology. Antigen-specific IL-10 secretion in peripheral blood of sheep exposed to Mptb was significantly higher than in control animals (P<0.001) as early as 4 months post-inoculation, and increased progressively. In ileal and jejunal lymph node cells, IL-10 secretion was also significantly higher in animals that were exposed to Mptb compared to controls (P<0.05). The early IL-10 response seen in peripheral blood cells may be a reflection of early responses at sites of Mptb infection. IL-10 secretion from ileal and jejunal lymph node cells was significantly higher in exposed animals with no lesions or with paucibacillary lesions when compared to animals with multibacillary lesions. These novel findings demonstrate that increased IL-10 activity commences soon after exposure to the causative mycobacterium and may play a role in determining disease outcome.
约内氏病是反刍动物的一种肠道分枝杆菌感染,对全球经济有重大影响。典型的宿主反应是早期T细胞介导的免疫反应,主要是干扰素γ(IFNγ)活性;随着动物进入疾病末期,这种反应随后会降低。白细胞介素(IL)-10可抑制Th1型并增强Th2型细胞因子的产生,被认为在约内氏病的后期起作用。为了确定IL-10在约内氏病整个病程中的作用,我们研究了无约内氏病(n = 10)、自然感染(n = 30)或实验感染(n = 58)的绵羊组。通过副结核分枝杆菌(Mptb)培养、组织病理学和血清学对动物的疾病状态进行了全面评估。早在接种后4个月,暴露于Mptb的绵羊外周血中抗原特异性IL-10分泌就显著高于对照动物(P<0.001),并逐渐增加。在回肠和空肠淋巴结细胞中,暴露于Mptb的动物与对照相比,IL-10分泌也显著更高(P<0.05)。外周血细胞中早期出现的IL-10反应可能反映了Mptb感染部位的早期反应。与有多菌型病变的动物相比,在无病变或有少菌型病变的暴露动物中,回肠和空肠淋巴结细胞的IL-10分泌显著更高。这些新发现表明,接触致病分枝杆菌后不久IL-10活性就会增加,并且可能在决定疾病结局中起作用。