Microbiome therapeutics for the treatment of recurrent Clostridioides difficile infection

被引:4
作者
Bloom, Patricia P. [1 ]
Young, Vincent B. [2 ,3 ,4 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Gastroenterol & Hepatol, Ann Arbor, MI USA
[2] Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI USA
[3] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI USA
[4] 1500 Med Ctr Dr, Ann Arbor, MI 48109 USA
关键词
C; difficile; microbiome; microbiome therapeutics; fecal microbiota transplant; OPEN-LABEL; TRANSPLANTATION; HEALTH; HOST; DIVERSITY; COLONIZATION; DETERMINANTS; PATHOGENESIS; DYSBIOSIS; EFFICACY;
D O I
10.1080/14712598.2022.2154600
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
IntroductionThe gut microbiome is implicated in Clostridioides difficile infection (CDI) and recurrent CDI (rCDI).Areas coveredThis review covers the mechanisms by which microbiome therapeutics treat rCDI, their efficacy and safety, and clinical trial design considerations for future research.Expert opinionAltering the chemical environment of the gut and reconstituting colonization resistance is a promising strategy for preventing and treating rCDI. Fecal microbiota transplant (FMT) is safe and effective for the treatment of rCDI. However, limitations of FMT have prompted investigation into alternative microbiome therapeutics. These alternative microbiome therapies require further evaluation, and adaptive trial designs should be strongly considered to more rapidly discern variables including the need for bowel preparation, timing and selection of pre-treatment antibiotics, and dose and duration of microbiome therapeutics. A broad range of adverse events must be prospectively evaluated in these controlled trials, as microbiome therapeutics have the potential for numerous effects. Future studies will lead to a greater understanding of the mechanisms by which microbiome therapies can break the cycle of rCDI, which should ultimately yield a personalized approach to rCDI treatment that restores an individual's specific deficit(s) in colonization resistance to C. difficile.
引用
收藏
页码:89 / 101
页数:13
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