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IL-6 positively regulates Foxp3+CD8+ T cells in vivo
Author(s) -
Takayuki Nakagawa,
Mineko Tsuruoka,
Hideki Ogura,
Yuko Okuyama,
Yasunobu Arima,
Toshio Hirano,
Masaaki Murakami
Publication year - 2009
Publication title -
international immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/dxp119
Subject(s) - foxp3 , cd8 , in vivo , inflammation , immunology , t cell , cytotoxic t cell , tcirg1 , microbiology and biotechnology , arthritis , chemistry , biology , cancer research , interleukin 21 , in vitro , immune system , biochemistry
Although recent studies have identified regulatory roles for Foxp3(+)CD8(+) T cells, the mechanisms that induce their development and underlie their functions in vivo have not been elucidated. Here, we show that IL-6 positively regulates the Foxp3(+)CD8(+) T-cell development and function. The Foxp3(+)CD8(+) T cells that differentiated in vitro in the presence of IL-6 suppressed autoimmune colitis and arthritis in vivo. Moreover, Foxp3(+)CD8(+) T cells that developed in vivo in the presence of enhanced IL-6 signaling suppressed the development of a spontaneous T(h)17 cell-mediated autoimmune arthritis. Thus, we concluded that Foxp3(+)CD8(+) T cells develop in response to IL-6 and regulate chronic inflammation in T(h)17 cell-mediated F759 autoimmune arthritis. These results suggested that Foxp3(+)CD8(+) T cells may develop in response to IL-6 under certain inflammatory conditions in vivo and may regulate some other chronic inflammation diseases.

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