Cutting edge:: CD8+CD122+ regulatory T cells produce IL-10 to suppress IFN-γ production and proliferation of CD8+ T cells
Cutting edge:: CD8+CD122+ regulatory T cells produce IL-10 to suppress IFN-γ production and proliferation of CD8+ T cells
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DOI:
10.4049/jimmunol.175.11.7093
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发表时间:
2005-12-01
影响因子:
4.4
通讯作者:
Suzuki, H
中科院分区:
文献类型:
--
作者:
Endharti, AT;Rifa'I, M;Suzuki, H
We recently identified CD8(+) CD122(+) regulatory T cells that directly control CD8(+) and CD4(+) cells without intervention of APCs. In this study, we investigated the effector mechanism of CD8+ CD122+ regulatory T cells by using an in vitro regulation system. The profile of cytokine expression revealed that IL-10 was predominantly produced by CD8(+) CD122(+) cells, whereas other cytokines were similarly expressed in CD8+ CD122+ cells and CD8(+) CD122(-) cells. Suppression of both proliferation CD122- cells by and IFN-gamma production by CD8, CD8(+) CD122(+) cells was blocked by adding anti-IL-10 Ab to the culture but not by adding anti-TGF-beta Ab. When IL-10 was removed from the conditioned medium from CD8(+) CD122(+) cells, the conditioned medium no longer showed regulatory activity. Finally, CD8(+) CD122(+) cells from IL-10-deficient mice had no regulatory activity in vitro and reduced regulatory activity in vivo. Our results clearly indicate that IL-10 is produced by CD8(+) CD122(+) cells and mediates the regulatory activity of these cells.