Jarrad Angie M, Karoli Tomislav, Blaskovich Mark A T, Lyras Dena, Cooper Matthew A
†The Institute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland 4072, Australia.
‡School of Biomedical Sciences, Monash University, Clayton, Victoria 3800, Australia.
J Med Chem. 2015 Jul 9;58(13):5164-85. doi: 10.1021/jm5016846. Epub 2015 Mar 30.
In the past decade Clostridium difficile has become a bacterial pathogen of global significance. Epidemic strains have spread throughout hospitals, while community acquired infections and other sources ensure a constant inoculation of spores into hospitals. In response to the increasing medical burden, a new C. difficile antibiotic, fidaxomicin, was approved in 2011 for the treatment of C. difficile-associated diarrhea. Rudimentary fecal transplants are also being trialed as effective treatments. Despite these advances, therapies that are more effective against C. difficile spores and less damaging to the resident gastrointestinal microbiome and that reduce recurrent disease are still desperately needed. However, bringing a new treatment for C. difficile infection to market involves particular challenges. This review covers the current drug discovery pipeline, including both small molecule and biologic therapies, and highlights the challenges associated with in vitro and in vivo models of C. difficile infection for drug screening and lead optimization.
在过去十年中,艰难梭菌已成为具有全球重要性的细菌病原体。流行菌株已在医院中广泛传播,而社区获得性感染及其他来源确保了孢子持续不断地接种到医院。为应对日益增加的医疗负担,一种新型艰难梭菌抗生素非达霉素于2011年获批用于治疗艰难梭菌相关性腹泻。初步的粪便移植也正在作为有效治疗方法进行试验。尽管有这些进展,但仍迫切需要更有效地对抗艰难梭菌孢子、对胃肠道常驻微生物群损害更小且能减少复发性疾病的疗法。然而,将一种针对艰难梭菌感染的新疗法推向市场面临着特殊挑战。本综述涵盖了当前的药物研发流程,包括小分子和生物疗法,并强调了与艰难梭菌感染的体外和体内模型用于药物筛选和先导化合物优化相关的挑战。