Wang Yifan, Hunt Aaron, Danziger Larry, Drwiega Emily N
Department of Pharmacy Practice, University of Illinois at Chicago College of Pharmacy, Chicago, IL 60612, USA.
Division of Infectious Diseases, University of Illinois at Chicago College of Medicine, Chicago, IL 60612, USA.
Antibiotics (Basel). 2024 May 12;13(5):436. doi: 10.3390/antibiotics13050436.
infection (CDI) is an intestinal infection that causes morbidity and mortality and places significant burden and cost on the healthcare system, especially in recurrent cases. Antibiotic overuse is well recognized as the leading cause of CDI in high-risk patients, and studies have demonstrated that even short-term antibiotic exposure can cause a large and persistent disturbance to human colonic microbiota. The recovery and sustainability of the gut microbiome after dysbiosis have been associated with fewer CDI recurrences. Fecal microbiota transplantation (FMT) refers to the procedure in which human donor stool is processed and transplanted to a patient with CDI. It has been historically used in patients with pseudomembranous colitis even before the discovery of . More recent research supports the use of FMT as part of the standard therapy of recurrent CDI. This article will be an in-depth review of five microbiome therapeutic products that are either under investigation or currently commercially available: Rebyota (fecal microbiota, live-jslm, formerly RBX2660), Vowst (fecal microbiota spores, live-brpk, formerly SER109), VE303, CP101, and RBX7455. Included in this review is a comparison of the products' composition and dosage forms, available safety and efficacy data, and investigational status.
艰难梭菌感染(CDI)是一种肠道感染,可导致发病和死亡,并给医疗系统带来巨大负担和成本,尤其是在复发病例中。抗生素的过度使用被公认为高危患者发生CDI的主要原因,并且研究表明,即使短期接触抗生素也会对人类结肠微生物群造成大规模且持续的干扰。生态失调后肠道微生物群的恢复和可持续性与较少的CDI复发相关。粪便微生物群移植(FMT)是指将人类供体粪便进行处理并移植给CDI患者的过程。甚至在发现[此处原文缺失相关内容]之前,它就已被用于治疗伪膜性结肠炎患者。最近的研究支持将FMT作为复发性CDI标准治疗的一部分。本文将对五种正在研究或目前已上市的微生物群治疗产品进行深入综述:Rebyota(粪便微生物群,活-jslm,原名RBX2660)、Vowst(粪便微生物群孢子,活-brpk,原名SER109)、VE303、CP101和RBX7455。本综述包括对这些产品的成分和剂型、可用的安全性和有效性数据以及研究状态的比较。