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Cutting edge: Induced indoleamine 2,3 dioxygenase expression in dendritic cell subsets suppresses T cell clonal expansion
被引:373
作者:
Mellor, AL
Baban, B
Chandler, P
Marshall, B
Jhaver, K
Hansen, A
Koni, PA
Iwashima, M
Munn, DH
机构:
[1] Med Coll Georgia, Inst Mol Med & Genet, Program Mol Immunol, Dept Med, Augusta, GA 30912 USA
[2] Med Coll Georgia, Inst Mol Med & Genet, Program Mol Immunol, Dept Pediat, Augusta, GA 30912 USA
[3] Lexicon Genet, The Woodlands, TX 77381 USA
[4] Res Ctr Allergy & Immunol, Inst Phys & Chem Res, Tsurumi Ku, Yokohama, Kanagawa, Japan
关键词:
D O I:
10.4049/jimmunol.171.4.1652
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
In mice, immunoregulatory APCs express the dendritic cell (DC) marker CD11c, and one or more distinctive markers (CD8alpha, B220, DX5). In this study, we show that expression of the tryptophan-degrading enzyme indoleamine 2,3 dioxygenase (IDO) is selectively induced in specific splenic DC subsets when mice were exposed to the synthetic immunomodulatory reagent CTLA4-Ig. CTLA4-Ig did not induce IDO expression in macrophages or lymphoid cells. Induction of IDO completely blocked clonal expansion of T cells from TCR transgenic mice following adoptive transfer, whereas CTLA4-Ig treatment did not block T cell clonal expansion in IDO-deficient recipients. Thus, IDO expression is an inducible feature of specific subsets of DO, and provides a potential mechanistic explanation for their T cell regulatory properties.
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页码:1652 / 1655
页数:4
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