Lerner Thomas R, Borel Sophie, Gutierrez Maximiliano G
Mill Hill Laboratory, The Francis Crick Institute, London, UK.
Cell Microbiol. 2015 Sep;17(9):1277-85. doi: 10.1111/cmi.12480. Epub 2015 Jul 28.
Mycobacterium tuberculosis (Mtb) infection can be cleared by the innate immune system before the initiation of an adaptive immune response. This innate protection requires a variety of robust cell autonomous responses from many different host immune cell types. However, Mtb has evolved strategies to circumvent some of these defences. In this mini-review, we discuss these host-pathogen interactions with a focus on studies performed in human cells and/or supported by human genetics studies (such as genome-wide association studies).
结核分枝杆菌(Mtb)感染在适应性免疫反应启动之前可被先天免疫系统清除。这种先天保护需要多种不同宿主免疫细胞类型产生强大的细胞自主反应。然而,Mtb已经进化出策略来规避其中一些防御机制。在这篇小型综述中,我们将讨论这些宿主-病原体相互作用,重点关注在人类细胞中进行的研究和/或得到人类遗传学研究(如全基因组关联研究)支持的研究。