Clostridium difficile--a moving target.

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-03-01 DOI:10.3410/M3-6
Glenn S Tillotson, Joni Tillotson
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引用次数: 18

Abstract

Clostridium difficile has been recognized as a pathogen in humans for over 40 years, but in the past decade the incidence has increased and, more importantly, the clinical presentation and consequences have become more serious, with increased morbidity and mortality. The emergence of a new, more pathogenic strain, BI/NAP1/027, has driven these shifts. Treatment of this disease has been with two antibiotics, metronidazole and vancomycin, but increasing recurrence, not uncommon with C. difficile infections, has prompted research into several alternative therapies. These include a new class of antibiotic (fidaxomicin), a monoclonal antibody, a vaccine, and most recently a biotherapeutic (which, in this case, is a nontoxin-producing strain of C. difficile). The future management of C. difficile infection will probably require a combination of these approaches once we have the data from ongoing studies.

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艰难梭菌——一个移动的目标。
艰难梭菌被认为是一种人类病原体已有40多年的历史,但在过去的十年中,其发病率有所增加,更重要的是,其临床表现和后果变得更加严重,发病率和死亡率都有所增加。一种新的、致病性更强的菌株BI/NAP1/027的出现推动了这些变化。这种疾病的治疗一直使用甲硝唑和万古霉素两种抗生素,但难辨梭菌感染的复发率越来越高,这促使人们研究几种替代疗法。其中包括一类新的抗生素(非达霉素),一种单克隆抗体,一种疫苗,以及最近的一种生物治疗药物(在这种情况下,是一种不产生毒素的艰难梭菌菌株)。一旦我们从正在进行的研究中获得数据,未来艰难梭菌感染的管理可能需要这些方法的组合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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