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From infection niche to therapeutic target: the intracellular lifestyle of Mycobacterium tuberculosis

机译:从感染利基到治疗目标:<斜体>结核分枝杆菌的细胞内生活方式

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Mycobacterium tuberculosis (Mtb) is an obligate human pathogen killing millions of people annually. Treatment for tuberculosis is lengthy and complicated, involving multiple drugs and often resulting in serious side effects and non-compliance. Mtb has developed numerous complex mechanisms enabling it to not only survive but replicate inside professional phagocytes. These mechanisms include, among others, overcoming the phagosome maturation process, inhibiting the acidification of the phagosome and inhibiting apoptosis. Within the past decade, technologies have been developed that enable a more accurate understanding of Mtb physiology within its intracellular niche, paving the way for more clinically relevant drug-development programmes. Here we review the molecular biology of Mtb pathogenesis offering a unique perspective on the use and development of therapies that target Mtb during its intracellular life stage.
机译:结核分枝杆菌(MTB)是每年杀死数百万人的迫长的人病原体。 对结核病的治疗是漫长而复杂的,涉及多种药物,通常导致严重的副作用和不合规。 MTB开发了许多复杂的机制,使其不仅活存,而且在专业吞噬细胞内复制。 这些机制包括克服吞噬蛋白酶成熟过程,抑制吞噬体的酸化并抑制细胞凋亡。 在过去十年中,已经开发了技术,使能够更准确地了解其细胞内利基内的MTB生理学,为更临床相关的药物开发计划铺平道路。 在这里,我们审查了MTB发病机制的分子生物学,提供了独特的视角,了解在其细胞内寿命期间靶向MTB的疗法的使用和开发。

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