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Murine Model of Epicutaneously-Induced Immunomodulation
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Heat-Killed Enterococcus faecalis EF-2001 Ameliorates Atopic Dermatitis in a Murine Model.
Eun-Ju Choi1, Masahiro Iwasa2, Kwon-Il Han3
1Division of Sport Science, College of Science and Technology, Konkuk University, Chungju 380-701, Korea. ooj7990@kku.ac.kr.
Nutrients
|March 10, 2016
Summary
Heat-killed Enterococcus faecalis EF-2001 (EF-2001) shows therapeutic potential for atopic dermatitis (AD). This study found EF-2001 effectively attenuated AD symptoms and reduced pathogenic cytokine expression in a mouse model.
Area of Science:
- Immunology
- Microbiology
- Dermatology
Background:
- Atopic dermatitis (AD) is an allergic skin condition linked to immune dysregulation.
- Heat-killed lactic acid bacteria are known for their immunomodulatory properties.
Purpose of the Study:
- To evaluate the therapeutic effect of heat-killed Enterococcus faecalis EF-2001 (EF-2001) on atopic dermatitis.
- To investigate the immunomodulatory mechanisms of EF-2001 in an in vivo AD model.
Main Methods:
- An in vivo atopic dermatitis (AD) model was created in mice using Dermatophagoides farinae extract (DFE) and 2,4-dinitrochlorobenzene (DNCB).
- Mice were orally administered EF-2001 for four weeks, followed by measurements of ear thickness, mast cell infiltration, and serum immunoglobulin levels.
- Gene expression of pathogenic cytokines in the ears, lymph nodes, and splenocytes was analyzed.
Main Results:
- EF-2001 administration significantly attenuated AD symptoms, as evidenced by reduced ear thickness and improved histopathological findings.
- Serum immunoglobulin levels, particularly IgE, were reduced in EF-2001 treated mice.
- EF-2001 decreased the expression of key pathogenic cytokines induced by DFE/DNCB in various tissues and immune cells.
Conclusions:
- Heat-killed Enterococcus faecalis EF-2001 demonstrates significant therapeutic potential for treating atopic dermatitis.
- The immunomodulatory effects of EF-2001 contribute to its efficacy in alleviating AD symptoms and reducing inflammatory responses.

