TY - JOUR
T1 - The induction of Treg cells by gut-indigenous Clostridium
AU - Nagano, Yuji
AU - Itoh, Kikuji
AU - Honda, Kenya
N1 - Funding Information:
This work was supported by the Japan Science and Technology Agency for Precursory Research for Embryonic Science and Technology (PRESTO) and the Japan Society for the Promotion of Science NEXT program .
PY - 2012/8
Y1 - 2012/8
N2 - Foxp3+ CD4+ cells are prominent immune regulatory T (Treg) cells that are most abundant in the intestine. Recent studies have suggested that intestinal Treg cells consist of thymically and extrathymically developed cells that have unique characteristics. A fraction of intestinal Treg cells express T cell receptors that recognize antigens that are derived from the gut microbiota. The presence of the gut microbiota, particularly the Clostridium species, affects the development and function of Treg cells. These intestinal bacteria-induced Treg cells are likely to play a role in the tolerance toward the gut microbiota. These recent advances provide new insight into how T cells are educated in the intestine to maintain homeostasis with the gut microbiota.
AB - Foxp3+ CD4+ cells are prominent immune regulatory T (Treg) cells that are most abundant in the intestine. Recent studies have suggested that intestinal Treg cells consist of thymically and extrathymically developed cells that have unique characteristics. A fraction of intestinal Treg cells express T cell receptors that recognize antigens that are derived from the gut microbiota. The presence of the gut microbiota, particularly the Clostridium species, affects the development and function of Treg cells. These intestinal bacteria-induced Treg cells are likely to play a role in the tolerance toward the gut microbiota. These recent advances provide new insight into how T cells are educated in the intestine to maintain homeostasis with the gut microbiota.
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U2 - 10.1016/j.coi.2012.05.007
DO - 10.1016/j.coi.2012.05.007
M3 - Review article
C2 - 22673877
AN - SCOPUS:84865296650
SN - 0952-7915
VL - 24
SP - 392
EP - 397
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
IS - 4
ER -