Hope Jayne C, Villarreal-Ramos Bernardo
Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, UK.
Comp Immunol Microbiol Infect Dis. 2008 Mar;31(2-3):77-100. doi: 10.1016/j.cimid.2007.07.003. Epub 2007 Aug 30.
Bovine tuberculosis (bTB) is caused by Mycobacterium bovis. The incidence of bTB is increasing in cattle herds of developed countries that have a wild life reservoir of M. bovis, such as the UK, New Zealand and the USA. The increase in the incidence of bTB is thought to be due, at least in part, to a wildlife reservoir of M. bovis. M. bovis is also capable of infecting humans and on a worldwide basis, M. bovis is thought to account for up to 10% of cases of human TB [Cosivi O, Grange JM, Daborn CJ et al. Zoonotic tuberculosis due to Mycobacterium bovis in developing countries. Emerg Infect Dis 1998;4(1):59-70]. Thus, the increased incidence of bTB, besides being a major economic problem, poses an increased risk to human health. In the UK, the incidence of bTB continues to rise despite the use of the tuberculin test and slaughter control policy, highlighting the need for improved control strategies. Vaccination of cattle, in combination with more specific and sensitive diagnostic tests, is suggested as the most effective strategy for bovine TB control. The only vaccine currently available for human and bovine TB is the live attenuated Bacille Calmette Guerin (BCG). BCG is thought to confer protection through the induction of Th1 responses against mycobacteria. However, protection against TB conferred by BCG is variable and to this date the reasons for the successes and failures of BCG are not clear. Therefore, there is a need to develop vaccines that confer greater and more consistent protection against bTB than that afforded by BCG. Given that BCG is currently the only licensed vaccine against human TB, it is likely that any new vaccine or vaccination strategy will be based around BCG. In this review we discuss immune responses elicited by mycobacteria in cattle and the novel approaches emerging for the control of bovine TB based on our increasing knowledge of protective immune responses.
牛结核病(bTB)由牛分枝杆菌引起。在存在牛分枝杆菌野生动物宿主的发达国家,如英国、新西兰和美国,牛群中牛结核病的发病率正在上升。牛结核病发病率的增加至少部分归因于牛分枝杆菌的野生动物宿主。牛分枝杆菌也能够感染人类,在全球范围内,牛分枝杆菌被认为占人类结核病病例的10%[科斯维O、格兰奇JM、达伯恩CJ等。发展中国家由牛分枝杆菌引起的人畜共患结核病。新发传染病杂志1998年;4(1):59 - 70]。因此,牛结核病发病率的增加除了是一个主要的经济问题外,还对人类健康构成了更大的风险。在英国,尽管使用了结核菌素试验和屠宰控制政策,但牛结核病的发病率仍在持续上升,这凸显了改进控制策略的必要性。建议对牛进行疫苗接种,并结合更特异、更灵敏的诊断检测,作为控制牛结核病的最有效策略。目前唯一可用于人类和牛结核病的疫苗是减毒活卡介苗(BCG)。卡介苗被认为通过诱导针对分枝杆菌的Th1反应来提供保护。然而,卡介苗对结核病的保护作用是可变的,迄今为止,卡介苗成功与失败的原因尚不清楚。因此,需要开发比卡介苗能提供更大、更一致的牛结核病保护作用的疫苗。鉴于卡介苗目前是唯一获得许可的抗人类结核病疫苗,任何新的疫苗或疫苗接种策略很可能都将以卡介苗为基础。在这篇综述中,我们根据对保护性免疫反应的不断了解,讨论牛体内分枝杆菌引发的免疫反应以及控制牛结核病的新出现的方法。