TY - JOUR
T1 - Induction of colonic regulatory T cells by indigenous Clostridium species
AU - Atarashi, Koji
AU - Tanoue, Takeshi
AU - Shima, Tatsuichiro
AU - Imaoka, Akemi
AU - Kuwahara, Tomomi
AU - Momose, Yoshika
AU - Cheng, Genhong
AU - Yamasaki, Sho
AU - Saito, Takashi
AU - Ohba, Yusuke
AU - Taniguchi, Tadatsugu
AU - Takeda, Kiyoshi
AU - Hori, Shohei
AU - Ivanov, Ivaylo I.
AU - Umesaki, Yoshinori
AU - Itoh, Kikuji
AU - Honda, Kenya
PY - 2011/1/21
Y1 - 2011/1/21
N2 - CD4+ T regulatory cells (Tregs), which express the Foxp3 transcription factor, play a critical role in the maintenance of immune homeostasis. Here, we show that in mice, Tregs were most abundant in the colonic mucosa. The spore-forming component of indigenous intestinal microbiota, particularly clusters IV and XIVa of the genus Clostridium, promoted Treg cell accumulation. Colonization of mice by a defined mix of Clostridium strains provided an environment rich in transforming growth factor-β and affected Foxp3+ Treg number and function in the colon. Oral inoculation of Clostridium during the early life of conventionally reared mice resulted in resistance to colitis and systemic immunoglobulin E responses in adult mice, suggesting a new therapeutic approach to autoimmunity and allergy.
AB - CD4+ T regulatory cells (Tregs), which express the Foxp3 transcription factor, play a critical role in the maintenance of immune homeostasis. Here, we show that in mice, Tregs were most abundant in the colonic mucosa. The spore-forming component of indigenous intestinal microbiota, particularly clusters IV and XIVa of the genus Clostridium, promoted Treg cell accumulation. Colonization of mice by a defined mix of Clostridium strains provided an environment rich in transforming growth factor-β and affected Foxp3+ Treg number and function in the colon. Oral inoculation of Clostridium during the early life of conventionally reared mice resulted in resistance to colitis and systemic immunoglobulin E responses in adult mice, suggesting a new therapeutic approach to autoimmunity and allergy.
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U2 - 10.1126/science.1198469
DO - 10.1126/science.1198469
M3 - Article
AN - SCOPUS:85027947787
SN - 0036-8075
VL - 331
SP - 337
EP - 341
JO - Science
JF - Science
IS - 6015
ER -