Kawamura Ikuo
Department of Microbiology, Kyoto University Graduate School of Medicine, Yoshidakonoe-cho, Sakyo-ku, Kyoto, Kyoto 606-8501, Japan.
Nihon Hansenbyo Gakkai Zasshi. 2008 Sep;77(3):219-24. doi: 10.5025/hansen.77.219.
Mycobacterium tuberculosis (MTB) is an intracellular pathogen that has evolved strategies to enable growth in macrophages. The bacterium is able to inhibit fusion of phagosomes with lysosomes through secretion of some bacterial components and modulation of host intracellular signaling pathways. Furthermore, it has been shown that phagositosed MTB is killed within macrophages after treatment with IFN-gamma in vitro. However, virulent MTB is capable of surviving in macrophages in vivo and persists in host even after acquired immunity has developed. These data suggest that MTB has developed a sophisticated immune evasion mechanism. In this issue, the strategies of MTB for intracellular survival and immune evasion, which have been unraveled so far, are shown and the mechanisms are discussed.
结核分枝杆菌(MTB)是一种细胞内病原体,它已经进化出在巨噬细胞中生长的策略。该细菌能够通过分泌一些细菌成分和调节宿主细胞内信号通路来抑制吞噬体与溶酶体的融合。此外,已有研究表明,体外经γ干扰素处理后,被吞噬的MTB在巨噬细胞内会被杀死。然而,毒力强的MTB能够在体内的巨噬细胞中存活,甚至在获得性免疫形成后仍能在宿主体内持续存在。这些数据表明MTB已经形成了一种复杂的免疫逃避机制。在本期中,展示了迄今为止已阐明的MTB细胞内存活和免疫逃避策略,并对其机制进行了讨论。