双歧杆菌
多糖
FOXP3型
微生物学
细胞
放线菌科
生物
化学
双歧杆菌
免疫学
免疫系统
细菌
细胞生物学
生物化学
乳酸菌
遗传学
作者
Ravi Verma,Changhon Lee,Eun-Ji Jeun,Jaeu Yi,Kwang Soon Kim,Ambarnil Ghosh,Seohyun Byun,Choong‐Gu Lee,Hye-Ji Kang,Gi-Cheon Kim,Chang‐Duk Jun,Gwénaël Jan,Chang‐Hee Suh,Ju‐Yang Jung,Jonathan Sprent,Dipayan Rudra,Cristina De Castro,Antonio Molinaro,Charles D. Surh,Sin‐Hyeog Im
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2018-10-19
卷期号:3 (28)
被引量:225
标识
DOI:10.1126/sciimmunol.aat6975
摘要
Dysregulation of intestinal microflora is linked to inflammatory disorders associated with compromised immunosuppressive functions of Foxp3+ T regulatory (Treg) cells. Although mucosa-associated commensal microbiota has been implicated in Treg generation, molecular identities of the "effector" components controlling this process remain largely unknown. Here, we have defined Bifidobacterium bifidum as a potent inducer of Foxp3+ Treg cells with diverse T cell receptor specificity to dietary antigens, commensal bacteria, and B. bifidum itself. Cell surface β-glucan/galactan (CSGG) polysaccharides of B. bifidum were identified as key components responsible for Treg induction. CSGG efficiently recapitulated the activity of whole bacteria and acted via regulatory dendritic cells through a partially Toll-like receptor 2-mediated mechanism. Treg cells induced by B. bifidum or purified CSGG display stable and robust suppressive capacity toward experimental colitis. By identifying CSGG as a functional component of Treg-inducing bacteria, our studies highlight the immunomodulatory potential of CSGG and CSGG-producing microbes.
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