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Exopolysaccharide from Lactobacillus rhamnosus KL37 Inhibits T Cell-dependent Immune Response in Mice
Bernadeta Nowak1, Małgorzata Śróttek1, Marta Ciszek-Lenda1
1Department of Immunology, Jagiellonian University Medical College, Czysta 18, 31-121, Kraków, Poland.
Archivum Immunologiae Et Therapiae Experimentalis
|May 26, 2020
Summary
Highly purified exopolysaccharides (EPS-37) from Lactobacillus rhamnosus KL37 ameliorate collagen-induced arthritis by suppressing T cell responses and reducing inflammatory markers. Intravenous administration proved most effective in reducing both symptoms and arthritogenic antibodies.
Area of Science:
- Immunology and Microbiology
- Bacterial Exopolysaccharides
- Inflammatory Disease Models
Background:
- Bacterial exopolysaccharides (EPSs) possess strain-specific immunomodulatory properties.
- Previous studies showed crude EPS from Lactobacillus rhamnosus KL37 ameliorated collagen-induced arthritis (CIA).
Purpose of the Study:
- To verify the anti-inflammatory properties of highly purified EPS from L. rhamnosus KL37 (EPS-37).
- To assess EPS-37's ability to suppress T cell-dependent humoral responses in a CIA model.
Main Methods:
- Active collagen-induced arthritis (CIA) model in mice immunized with type II collagen (CII) and lipopolysaccharide (LPS).
- Treatment with purified EPS-37 via intravenous and subcutaneous routes.
- Ex vivo and in vitro assessment of T-cell proliferation and cytokine production (Interferon-gamma [IFN-γ]).
Main Results:
- Intravenous EPS-37 markedly ameliorated arthritis and reduced CII-specific antibody production.
- Subcutaneous EPS-37 reduced clinical arthritis symptoms but not arthritogenic antibodies.
- EPS-37 inhibited T-cell proliferation and reduced IFN-γ production.
Conclusions:
- EPS-37 exhibits anti-inflammatory potential by inhibiting Th1-mediated inflammatory pathways.
- L. rhamnosus KL37 EPS may be useful for controlling T cell-dependent immune responses in inflammatory diseases.
- Optimal administration route for EPS-37 requires tailoring for specific disorders.
Keywords:
Collagen-induced arthritisExopolysaccharideImmunomodulationInflammationLactobacillus rhamnosusT cells
