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Antimicrobial Peptides and Peptidomimetics - Potent Therapeutic Allies for Staphylococcal Infections

机译:抗菌肽和拟肽-葡萄球菌感染的强效治疗同盟

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摘要

The pervasiveness of bacterial resistance to conventional antibiotics, particularly those associated with staphylococcal infections, has become a global epidemic. However, research involving antimicrobial peptides (AMPs) and their synthetic analogues has unearthed a potentially novel class of antibacterials for the treatment of an array of diseases caused by pathogenic bacteria, such as staphylococci. AMPs have several unique advantages over traditional antibiotics such as the projected slow emergence of bacterial resistance to these agents and their capability to modulate the host immune response to infection. Unfortunately, their susceptibility to proteolytic degradation, loss of antimicrobial activity due to serum binding or physiological concentration of salts, and toxicity to host tissues has limited their use as systemic agents thus far. Additionally, the presence of economic and regulatory obstacles has hindered the translation of AMPs, as antimicrobials, from the bench to the clinic. The present review delves further into the benefits and challenges of utilizing AMPs as antibacterial agents (particularly for staphylococcal infections), the methods which have been utilized to overcome their limitations, their successes and failures in clinical trials, and future avenues for researchers to pursue to develop AMPs as novel therapeutic allies in the treatment of bacterial infections.
机译:细菌对常规抗生素,特别是与葡萄球菌感染相关的抗生素的耐药性普遍存在,已成为全球流行病。但是,涉及抗菌肽(AMPs)及其合成类似物的研究已经发现了潜在的新型抗菌剂,用于治疗由病原菌引起的一系列疾病,例如葡萄球菌。与传统抗生素相比,AMP具有几个独特的优势,例如细菌对这些药剂的耐药性预计会缓慢出现,并具有调节宿主对感染的免疫反应的能力。不幸的是,迄今为止,它们对蛋白水解降解的敏感性,由于血清结合或盐的生理浓度引起的抗微生物活性的丧失以及对宿主组织的毒性限制了它们作为全身剂的用途。此外,经济和监管方面的障碍也阻碍了AMPs作为抗菌剂从实验室到临床的转化。本综述进一步探讨了使用AMPs作为抗菌剂(尤其是用于葡萄球菌感染)的好处和挑战,已被用来克服其局限性的方法,它们在临床试验中的成功和失败以及研究人员追求的未来途径。发展AMPs作为治疗细菌感染的新型治疗同盟。

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