Asthma Prevention by Lactobacillus Rhamnosus in a Mouse Model is Associated With CD4+CD25+Foxp3+ T Cells.
10.4168/aair.2012.4.3.150
- Author:
Seong Ok JANG
1
;
Ha Jung KIM
;
Young Joon KIM
;
Mi Jin KANG
;
Ji Won KWON
;
Ju Hee SEO
;
Hyung Young KIM
;
Byoung Ju KIM
;
Jinho YU
;
Soo Jong HONG
Author Information
1. Asan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Asthma;
probiotics;
mice;
T-lymphocytes, Regulatory
- MeSH:
Administration, Oral;
Animals;
Asthma;
Bacteria;
Cytokines;
Eosinophils;
Immune Tolerance;
Immunoglobulin E;
Inflammation;
Interleukin-5;
Lactobacillus;
Lactobacillus rhamnosus;
Lymphocytes;
Mice;
Negotiating;
Probiotics;
Spleen;
T-Lymphocytes;
T-Lymphocytes, Regulatory
- From:Allergy, Asthma & Immunology Research
2012;4(3):150-156
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Probiotic bacteria can induce immune regulation or immune tolerance in allergic diseases. The underlying mechanisms have been recently investigated, but are still unclear. The aim of this study was to evaluate the protective effects of the probiotic Lactobacillus rhamnosus (Lcr35) in a mouse model of asthma and to identify its mechanism of action. METHODS: Lcr35 was administered daily by the oral route at a dosage of 1x10(9) CFU/mouse in BALB/c mice for 7 days before the first sensitization. Clinical parameters and regulatory T (Treg) cells were examined. The role of CD4+CD25+Foxp3+ Treg cells was analyzed using a Treg cell-depleting anti-CD25 monoclonal antibody (mAb). RESULTS: Airway hyperresponsiveness, total IgE production, pulmonary eosinophilic inflammation, and splenic lymphocyte proliferation were suppressed after Lcr35 treatment. Th1 (IFN-gamma) and Th2 (IL-4, IL-5, and IL-13) cytokines in the serum were suppressed, and the percentage of CD4+CD25+Foxp3+ Treg cells in the spleen was significantly increased in the Lcr35 treatment group. Anti-CD25 mAb administration abolished the protective effects of Lcr35, indicating that CD4+ CD25+Foxp3+ Treg cells are essential in mediating the activity of Lcr35. CONCLUSIONS: Oral administration of Lcr35 attenuated the features of allergic asthma in a mouse model and induced immune regulation by a CD4+CD25+Foxp3+ Treg cell-mediated mechanism.
