Andersen Peter
Department of Infectious Disease Immunology, Statens Serum Institute, DK-2300 Copenhagen, Denmark.
Trends Microbiol. 2007 Jan;15(1):7-13. doi: 10.1016/j.tim.2006.11.008. Epub 2006 Dec 1.
The leading tuberculosis (TB) vaccines currently in clinical trials are all designed as prophylactic vaccines. Although these vaccines are highly active, they will most probably not result in sterilizing immunity and, therefore, will not solve the global problem of latent TB. An attractive strategy is to target the remaining dormant bacteria with vaccines based upon antigens induced as the bacteria change from active multiplication to non-replicating dormancy (latency antigens) or during reactivation as dormant bacteria resume active metabolism (resuscitation antigens). These late-stage antigens might have potential as post-exposure vaccines or could form the basis for a multi-stage vaccine strategy, in which they are combined with prophylactic vaccines based on early antigens from replicating bacteria.
目前处于临床试验阶段的主要结核病(TB)疫苗均设计为预防性疫苗。尽管这些疫苗具有高度活性,但很可能无法产生灭菌免疫,因此无法解决全球潜伏性结核病问题。一种有吸引力的策略是,基于细菌从活跃增殖转变为非复制性休眠(潜伏抗原)或休眠细菌恢复活跃代谢(复苏抗原)过程中诱导产生的抗原,用疫苗靶向剩余的休眠细菌。这些后期抗原可能具有作为暴露后疫苗的潜力,或者可以形成多阶段疫苗策略的基础,即将它们与基于复制细菌早期抗原的预防性疫苗相结合。