Effect of the probiotic Weissella cibaria CMS1 on the immune response and the oral microbiome: a randomized, double-blind, placebo-controlled, parallel study.
Min Ju ParkSoo-Yeon ParkKyeong Jin KimBumjo OhJi Yeon KimPublished in: Food & function (2024)
The oral cavity connects the external environment and the respiratory and digestive systems, and the oral microbial ecosystem is complex and plays a crucial role in overall health and immune defense against external threats. Recently, the potential use of probiotics for disease prevention and treatment has gained attention. This study aimed to assess the effect of Weissella cibaria CMS1 ( W. cibaria CMS1) consumption on the oral microbiome and immune function in healthy individuals through a 12-week clinical trial. This randomized, double-blind, placebo-controlled, parallel trial enrolled 90 healthy subjects. The consumption of W. cibaria CMS1 significantly increased salivary immunoglobulin A ( p = 0.046) and decreased tumor necrosis factor-α (TNF-α) levels ( p = 0.008). Analysis of the oral microbiota revealed changes in beta diversity, increased abundance of Firmicutes and Actinobacteria, and decreased abundance of Bacteroidetes and Fusobacteria after 12 weeks of consuming W. cibaria CMS1. Significant increases in various strains, including Lactobacillales, Bacilli, Streptococcaceae, Streptococcus, and Firmicutes, were observed in the W. cibaria CMS1 group after 12 weeks of intake. Additionally, Fusobacteriia Fusobacteriales Fusobacteriaceae and Fusobacteriia Fusobacteriales Fusobacteriaceae Fusobacterium exhibited a positive correlation with TNF-α. These findings demonstrate the positive effect of W. cibaria CMS1 on the oral environment and immune function.
Keyphrases
- placebo controlled
- double blind
- phase iii
- clinical trial
- phase ii
- study protocol
- immune response
- phase ii study
- rheumatoid arthritis
- open label
- public health
- human health
- randomized controlled trial
- microbial community
- squamous cell carcinoma
- risk assessment
- cystic fibrosis
- dendritic cells
- multidrug resistant
- toll like receptor
- respiratory tract