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Molecular Mechanisms of Host-Pathogen Interactions and their Potential for the Discovery of New Drug Targets

机译:宿主-病原菌相互作用的分子机制及其发现新药靶标的潜力

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摘要

Vaccines and chemotherapy have undeniably been the discoveries in the field of biomedical research that havenexerted the biggest impact on the improvement of public health. Nevertheless, the development of bacterial resistance tonantibiotics has co-evolved over time with the discovery of new drugs. This entails the necessity for continuous research onnnew anti-infectious agents.The current review highlights recent discoveries in the molecular mechanisms of specific hostnpathogen interactions and their potential for drug discovery. The focus is on facultative and obligate intracellular pathogensn(Mycobacterium, Chlamydia and Legionella) and their manipulation of host cells in regard to inhibition ofnphagosome maturation and cell death. Furthermore, the composition and role of the SecA2 and the ESX-1 secretion pathwaysnin bacterial virulence and manipulation of infected host cells is discussed. The central hypothesis proposed in thisnreview is that the characterization of bacterial proteins and lipids involved in host cell manipulation (modulins) will providenan abundance of new drug targets. One advantage of targeting such bacterial modulins for drug development is thatnthese anti-modulin drugs will not disrupt the beneficial host microflora and therefore have fewer side effects.
机译:毫无疑问,疫苗和化学疗法是生物医学研究领域中对改善公共卫生影响最大的发现。然而,随着新药的发现,细菌抗性tonantibiotics的发展随着时间的发展而共同发展。因此,有必要对新的抗感染药进行持续研究。本综述着重介绍了特定宿主病原体相互作用的分子机制及其在药物发现中的潜力的最新发现。重点是兼性和专性的细胞内病原体(分枝杆菌,衣原体和军团菌)及其对宿主细胞的操纵,以抑制吞噬体的成熟和细胞死亡。此外,讨论了SecA2和ESX-1分泌途径在细菌毒力和感染宿主细胞操纵中的组成和作用。本综述提出的主要假设是,参与宿主细胞操作(调节素)的细菌蛋白质和脂质的表征将提供大量新药靶标。靶向这种细菌调节蛋白用于药物开发的一个优点是,这些抗调节蛋白药物不会破坏有益的宿主菌群,因此副作用较小。

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