| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6087749 | Clinical Immunology | 2012 | 10 Pages |
Lactic acid bacteria have potential in immunomodulation therapy, but their clinical efficacy and underlying mechanisms are unclear. We aimed to clarify the anti-allergic immune responses induced by intragastric and sublingual administration of heat-killed Lactobacillus paracasei KW3110 and Lactobacillus acidophilus L-92. The KW3110 strain (but not the L-92 strain) enhanced ovalbumin (OVA)-induced expression of CCR-7 and PD-L2 in murine dendritic cells (DCs), and strongly inhibited IL-5 and IL-13 production in vitro in co-cultures with Th2-skewed CD4+ T cells from DO11.10 transgenic mice. Sublingual administration of low-dose KW3110 (but not L-92) to OVA-sensitized mice selectively suppressed serum IgE production and Th2 cytokine expression in cervical lymph nodes, and significantly improved symptoms after OVA provocation in vivo. KW3110 probably accelerates DC migration into the regional lymph nodes and inhibits Th2 cytokine production through enhanced CCR-7 and PD-L2 expression. Thus, sublingual KW3110 administration may be effective in reducing allergic inflammation.
⺠Sublingual Lactobacillus paracasei KW3110 therapy may reduce allergic inflammation. ⺠This occurs by Th2 cytokine inhibition through enhanced CCR-7 and PD-L2 expression. ⺠Subcutaneous or sublingual Lactobacillus paracasei L-92 therapy was ineffective. ⺠Simultaneous antigen stimulation may enhance the anti-allergic effects of KW3110.
