| Literature DB >> 16301610 |
Agustina Tri Endharti1, Muhaimin Rifa'I, Zhe Shi, Yukari Fukuoka, Yoshio Nakahara, Yoshiyuki Kawamoto, Kozue Takeda, Ken-Ichi Isobe, Haruhiko Suzuki.
Abstract
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 and IFN-gamma production by CD8+CD122- cells by 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.Entities:
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Year: 2005 PMID: 16301610 DOI: 10.4049/jimmunol.175.11.7093
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422