Gut microbiota changes associated with Clostridioides difficile infection and its various treatment strategies

被引:27
|
作者
Gonzales-Luna, Anne J. [1 ]
Carlson, Travis J. [2 ]
Garey, Kevin W. [1 ,3 ]
机构
[1] Univ Houston, Coll Pharm, Dept Pharm Practice & Translat Res, Houston, TX USA
[2] High Point Univ, Fred Wilson Sch Pharm, Dept Clin Sci, High Point, NC USA
[3] Univ Houston, Coll Pharm, Dept Pharm Practice & Translat Res, 4349 Martin Luther King Blvd,HBS2 Bldg,Room 4039, Houston, TX 77204 USA
关键词
Microbiome; microbiota; Clostridium difficile; Clostridioides difficile; antibiotic-associated dysbiosis; live biotherapeutic product; Firmicutes; metronidazole; vancomycin; fidaxomicin; HEALTH-CARE EPIDEMIOLOGY; CLINICAL-PRACTICE GUIDELINE; FOCUSED UPDATE GUIDELINES; FECAL MICROBIOTA; OPEN-LABEL; DISEASES SOCIETY; AMERICA IDSA; BILE-ACIDS; VANCOMYCIN; TRANSPLANTATION;
D O I
10.1080/19490976.2023.2223345
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Human gut microbiota are critical to both the development of and recovery from Clostridioides difficile infection (CDI). Antibiotics are the mainstay of CDI treatment, yet inherently cause further imbalances in the gut microbiota, termed dysbiosis, complicating recovery. A variety of microbiota-based therapeutic approaches are in use or in development to limit disease- and treatment-associated dysbiosis and improve rates of sustained cure. These include the recently FDA-approved fecal microbiota, live-jslm (formerly RBX2660) and fecal microbiota spores, live-brpk (formerly SER-109), which represent a new class of live biotherapeutic products (LBPs), traditional fecal microbiota transplantation (FMT), and ultra-narrow-spectrum antibiotics. Here, we aim to review the microbiome changes associated with CDI as well as a variety of microbiota-based treatment approaches.
引用
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页数:13
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