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Updated: Aug 1, 2026

Detection of Enterohemorrhagic Escherichia Coli Colonization in Murine Host by Non-invasive In Vivo Bioluminescence System
Published on: April 9, 2018
[Immunomodulator action of living, nonpathogenic Enterococcus faecalis bacteria from humans]
1INLUPA-Institut für Lebensmitteluntersuchungen, Umwelthygiene und Pharmakaanalytik GmbH, Mönchengladbach.
Living nonpathogenic Enterococcus faecalis (E. faecalis) modulates immune responses by stimulating cytokine release, including interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6). These effects are dose-dependent and influenced by specific inhibitors, suggesting therapeutic potential.
Area of Science:
- Immunology
- Microbiology
- Pharmacology
Background:
- Symbioflor 1 contains living nonpathogenic Enterococcus faecalis (E. faecalis).
- Cytokines play a crucial role in immune system regulation.
- Understanding microbial-host interactions is key to developing immunomodulatory therapies.
Purpose of the Study:
- To investigate the immunomodulatory effects of E. faecalis on human peripheral mononuclear blood cells.
- To determine the impact of E. faecalis on cytokine liberation in vitro.
- To explore the influence of dexamethasone and cyclosporin A on E. faecalis-induced cytokine production.
Main Methods:
- In vitro experiments using human peripheral mononuclear blood cells.
- Dose-dependent assessment of cytokine liberation (IL-1 beta, IL-6, IFN-gamma, IL-2).
- Evaluation of inhibitory effects of dexamethasone (Dm) and cyclosporin A (CsA) on cytokine production.
Main Results:
- E. faecalis stimulated dose-dependent liberation of IL-1 beta and IL-6, inhibited by Dm but not CsA.
- E. faecalis stimulated dose-dependent liberation of gamma-interferon (IFN-gamma), inhibited by both Dm and CsA.
- E. faecalis inhibited phytohemagglutinin (PHA)-induced IFN-gamma and IL-2 liberation in a dose-dependent manner.
Conclusions:
- E. faecalis exhibits significant immunomodulatory activity by influencing cytokine profiles.
- The differential inhibition by Dm and CsA suggests distinct signaling pathways involved.
- In vitro findings provide a basis for further investigation in clinical trials for immunomodulatory applications.
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