Microbiota restoration therapies for recurrent Clostridioides difficile infection reach an important new milestone

被引:3
|
作者
Dupont, Herbert L. [1 ,2 ,3 ,6 ]
Dupont, Andrew W. [4 ]
Tillotson, Glenn S. [5 ]
机构
[1] Univ Texas McGovern Med Sch, Dept Internal Med, Houston, TX USA
[2] Baylor Coll Med, Dept Med, Houston, TX USA
[3] Kelsey Res Fdn, Houston, TX USA
[4] Univ Texas Hlth Sci Ctr Houston, Div Gastroenterol, Houston, TX USA
[5] GST Micro LLC, North, VA USA
[6] Univ Texas Sch Publ Hlth, Dept Epidemiol, Infect Dis & Epidemiol, 1200 Pressler St, Houston, TX 77030 USA
关键词
Clostridioides difficile; fecal microbiota transplantation; live biotherapeutic products; REBYOTA (TM); VOWST; TRANSPLANTATION; SER-109;
D O I
10.1177/17562848241253089
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Microbiota restoration therapy has become a standard treatment for recurrent Clostridioides difficile infection (rCDI). In this article, we review the studies supporting the licensure of two live biotherapeutic products (LBPs) designed to prevent rCDI and to provide clinicians with a perspective on their differences. PubMed was reviewed on 1 October 2023, for all papers published concerning the current Food and Drug Administration allowance of the use of fecal microbiota transplantation (FMT) and the studies that led to the licensure of RBX2660 (REBYOTA (TM)), generic name, fecal microbiota, live-jslm, and SER-109 (VOWST (TM)), generic name, fecal microbiota spores, live-brpk. OpenBiome continues to produce fecal products for patients with rCDI at their treatment sites, and the American Gastroenterology Association has a National Registry focused on long-term safety of administering fecal microbiota products. The science behind the licensing of fecal microbiota, live-jslm, a consortium of fecal anaerobes found in stool augmented with strains of Bacteroidetes and fecal microbiota spores, live-brpk, a mixture of 50 species of purified Firmicutes spores is reviewed. Both products appear to be safe in clinical trials and effective in reducing rCDI episodes by mechanisms established for FMT, including normalization of alpha- and beta-diversity of the microbiome and by increasing fecal secondary bile acids. The different makeup of the two LBPs suggests that rCDI responds to a variety of engrafting microbiota which explains why nearly all donors in FMT of rCDI are generally effective. Fecal microbiota, live-jslm has also been shown to successfully treat rCDI in elderly patients with advanced comorbidities. With the licensure of two novel LBPs, we are entering a new phase of microbiota replacement therapy. Having standardized manufacturing and proper monitoring of products, harnessing the microbiome to control and prevent disease has a new beginning.
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页数:11
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