Literature DB >> 23982236

Clostridium difficile: biological therapies.

Jessica Martin1, Damian Mawer, Mark H Wilcox.   

Abstract

PURPOSE OF REVIEW: Biological therapies for Clostridium difficile infection (CDI) include probiotics and faecal microbiota transplant (FMT). There is significant interest in their use in treating refractory/recurrent CDI. This review summarizes the latest evidence for these approaches. RECENT
FINDINGS: The small number of randomized controlled trials (RCTs) using probiotics in CDI have produced variable results; the most recent showed no benefit in preventing disease. However, several meta-analyses published in the last year have suggested benefit in their use, but these conclusions are limited by the poor quality of many of the primary studies, and lack of standardization of the probiotic administered. In contrast, FMT appears highly effective for the treatment of CDI. In the only published RCT, the cure rate was 81%, which is close to the rate shown by meta-analyses of previous case series. The use of artificially produced bacterial mixtures in place of faecal samples is now under investigation.
SUMMARY: Biological therapies for CDI, especially FMT, will continue to attract attention. Further, large-scale RCTs are required to identify which patients are most likely to benefit from these therapies in the future.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23982236     DOI: 10.1097/01.qco.0000433319.82618.8f

Source DB:  PubMed          Journal:  Curr Opin Infect Dis        ISSN: 0951-7375            Impact factor:   4.915


  2 in total

1.  Clostridium difficile recurrence is characterized by pro-inflammatory peripheral blood mononuclear cell (PBMC) phenotype.

Authors:  Mary B Yacyshyn; Tara N Reddy; Lauren R Plageman; Jiang Wu; Amy R Hollar; Bruce R Yacyshyn
Journal:  J Med Microbiol       Date:  2014-07-07       Impact factor: 2.472

2.  Screening of Bifidobacteria and Lactobacilli Able to Antagonize the Cytotoxic Effect of Clostridium difficile upon Intestinal Epithelial HT29 Monolayer.

Authors:  Lorena Valdés-Varela; Marta Alonso-Guervos; Olivia García-Suárez; Miguel Gueimonde; Patricia Ruas-Madiedo
Journal:  Front Microbiol       Date:  2016-04-22       Impact factor: 5.640

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.