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Addressing Latent Tuberculosis: New Advances in Mimicking the Disease Discovering Key Targets and Designing Hit Compounds

机译:解决潜在结核病:模仿疾病的新进展发现关键目标并设计击中化合物

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摘要

Despite being discovered and isolated more than one hundred years ago, tuberculosis (TB) remains a global public health concern arch. Our inability to eradicate this bacillus is strongly related with the growing resistance, low compliance to current drugs, and the capacity of the bacteria to coexist in a state of asymptomatic latency. This last state can be sustained for years or even decades, waiting for a breach in the immune system to become active again. Furthermore, most current therapies are not efficacious against this state, failing to completely clear the infection. Over the years, a series of experimental methods have been developed to mimic the latent state, currently used in drug discovery, both in vitro and in vivo. Most of these methods focus in one specific latency inducing factor, with only a few taking into consideration the complexity of the granuloma and the genomic and proteomic consequences of each physiological factor. A series of targets specifically involved in latency have been studied over the years with promising scaffolds being discovered and explored. Taking in account that solving the latency problem is one of the keys to eradicate the disease, herein we compile current therapies and diagnosis techniques, methods to mimic latency and new targets and compounds in the pipeline of drug discovery.
机译:尽管被发现并孤立了超过一百年前,但结核病(TB)仍然是全球公共卫生关注的拱门。我们无法消除该杆菌与肺部抗性,低对当前药物的血糖效果低,以及细菌在无症状等延迟的状态下共存的能力强烈相关。最后一个州可以持续多年甚至数十年,等待免疫系统中的违约,再次变得活跃。此外,大多数当前疗法对这种状态没有有效,不能完全清楚感染。多年来,已经开发了一系列实验方法来模仿目前在药物发现中使用的潜在状态,两者在体外和体内使用。这些方法中的大多数侧重于一个特定的潜伏期诱导因子,只考虑肉芽肿的复杂性以及每个生理因素的基因组和蛋白质组后果。多年来,一系列专门参与延迟的目标,并且有前途的脚手架被发现和探索。考虑到解决潜伏期问题是消除疾病的键之一,在此我们编制了当前的疗法和诊断技术,用于模拟潜伏期和药物发现管道中的新目标和化合物的方法。

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