| Literature DB >> 36012597 |
Lisa Danielly Curcino Araujo1, Flávia Aparecida Chaves Furlaneto2, Léa Assed Bezerra da Silva1, Yvonne L Kapila3.
Abstract
The oral cavity is one of the environments on the human body with the highest concentrations of microorganisms that coexist harmoniously and maintain homeostasis related to oral health. Several local factors can shift the microbiome to a pathogenic state of dysbiosis. Existing treatments for infections caused by changes in the oral cavity aim to control biofilm dysbiosis and restore microbial balance. Studies have used probiotics as treatments for oral diseases, due to their ability to reduce the pathogenicity of the microbiota and immunoinflammatory changes. This review investigates the role of the probiotic Bifidobacterium animalis subsp. lactis (B. lactis) HN019 in oral health, and its mechanism of action in pre-clinical and clinical studies. This probiotic strain is a lactic acid bacterium that is safe for human consumption. It mediates bacterial co-aggregation with pathogens and modulates the immune response. Studies using B. lactis HN019 in periodontitis and peri-implant mucositis have shown it to be a potential adjuvant treatment with beneficial microbiological and immunological effects. Studies evaluating its oral effects and mechanism of action show that this probiotic strain has the potential to be used in several dental applications because of its benefit to the host.Entities:
Keywords: dysbiosis; endodontics; oral health; periodontitis; probiotic
Mesh:
Year: 2022 PMID: 36012597 PMCID: PMC9409207 DOI: 10.3390/ijms23169334
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 6.208
Figure 1Representative figure of an epithelial cell and its interactions with the microbiome.
Studies using the B. lactis HN019 strain in the context of periodontitis.
| Administration | Type of Study | Dosage/Time | Result | Reference |
|---|---|---|---|---|
| 10% skimmed milk (Molico®, Nestle Brasil Ltd.a., São Paulo, SP, Brazil) plus | Preclinical in rats | 1.9 × 109; 15 days | Oral use of | Ricoldi et al., 2017 [ |
| Suspension containing | Preclinical in rats | 1.9 × 109; 0, 3 and 7 days | Topical use of | Oliveira et al., 2017 [ |
| Preclinical in rats | 1.9 × 109; 4 weeks | Oliveira et al., 2022-a [ | ||
| Preclinical in rat | 1 × 109; 4 weeks | Oliveira et al., 2022-b [ | ||
| B. | Preclinical in rats | 1.5 × 109; 39 days | Systemic administration of | Cardoso et al., 2020 [ |
| Preclinical in rats | 1 × 109; 8 weeks | Silva et al., 2022 [ | ||
| Randomized clinical trial | 109; 30 days | Ancillary treatment with | Invernici et al., 2018 [ | |
| Randomized clinical trial and in vitro analysis | 109; 30 days | Invernici et al., 2020 [ |
Figure 2The effects of B. lactis HN19 on periodontitis.