Mucosal T Cells Expressing High Levels of IL-7 Receptor Are Potential Targets for Treatment of Chronic Colitis
Author(s) -
Motomi Yamazaki,
Tomoharu Yajima,
M. Tanabe,
Kazuto Fukui,
Eriko Okada,
Ryuichi Okamoto,
Shigeru Oshima,
Tetsuya Nakamura,
Takanori Kanai∥,
Masahiro Uehira,
Tsutomu Takeuchi,
Hiromichi Ishikawa,
Toshifumi Hibi∥,
Mamoru Watanabe
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.171.3.1556
Subject(s) - colitis , inflammatory bowel disease , immunology , inflammation , transgene , immune system , genetically modified mouse , intestinal mucosa , t cell receptor , medicine , biology , t cell , cancer research , disease , pathology , gene , biochemistry
The IL-7/IL-7R-dependent signaling pathway plays a crucial role in regulating the immune response in intestinal mucosa. Here we demonstrate the pivotal role of this pathway in the development and treatment of chronic colitis. T cells expressing high levels of IL-7R were substantially infiltrated in the chronic inflamed mucosa of TCR alpha-chain knockout mice and IL-7 transgenic mice. Transfer of mucosal T cells expressing high levels of IL-7R, but not T cells expressing low levels of IL-7R, from these mice into recombinase-activating gene-2(-/-) mice induced chronic colitis. Selective elimination of T cells expressing high levels of IL-7R by administrating small amounts of toxin-conjugated anti-IL-7R Ab completely ameliorated established, ongoing colitis. These findings provide evidence that therapeutic approaches targeting mucosal T cells expressing high levels of IL-7R are effective in the treatment of chronic intestinal inflammation and may be feasible for use in the therapy of human inflammatory bowel disease.
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