Generation of regulatory dendritic cells and CD4 <sup>+</sup> Foxp3 <sup>+</sup> T cells by probiotics administration suppresses immune disorders

Ho‐Keun Kwon(Gwangju Institute of Science and Technology), Choong‐Gu Lee(Gwangju Institute of Science and Technology), Jae‐Seon So(Gwangju Institute of Science and Technology), Chang-Suk Chae(Gwangju Institute of Science and Technology), Ji-Sun Hwang(Gwangju Institute of Science and Technology), Anupama Sahoo(Gwangju Institute of Science and Technology), Jong Hee Nam(Chonnam National University), Joon Haeng Rhee(Chonnam National University), Ki-Chul Hwang(Yonsei University), Sin‐Hyeog Im(Gwangju Institute of Science and Technology)
Proceedings of the National Academy of Sciences
January 13, 2010
Cited by 589Open Access
Full Text

Abstract

The beneficial effects of probiotics have been described in many diseases, but the mechanism by which they modulate the immune system is poorly understood. In this study, we identified a mixture of probiotics that up-regulates CD4(+)Foxp3(+) regulatory T cells (Tregs). Administration of the probiotics mixture induced both T-cell and B-cell hyporesponsiveness and down-regulated T helper (Th) 1, Th2, and Th17 cytokines without apoptosis induction. It also induced generation of CD4(+)Foxp3(+) Tregs from the CD4(+)CD25(-) population and increased the suppressor activity of naturally occurring CD4(+)CD25(+) Tregs. Conversion of T cells into Foxp3(+) Tregs is directly mediated by regulatory dendritic cells (rDCs) that express high levels of IL-10, TGF-beta, COX-2, and indoleamine 2,3-dioxygenase. Administration of probiotics had therapeutical effects in experimental inflammatory bowel disease, atopic dermatitis, and rheumatoid arthritis. The therapeutical effect of the probiotics is associated with enrichment of CD4(+)Foxp3(+) Tregs in the inflamed regions. Collectively, the administration of probiotics that enhance the generation of rDCs and Tregs represents an applicable treatment of inflammatory immune disorders.


Related Papers

No related papers found

Powered by citation graph analysis