CD8+CD122+ regulatory T cells recognize activated T cells via conventional MHC class I-αβTCR interaction and become IL-10-producing active regulatory cells

被引:83
作者
Rifa'i, Muhaimin [1 ,2 ]
Shi, Zhe [1 ]
Zhang, Shu-Yun [3 ]
Lee, Young Ho [1 ]
Shiku, Hiroshi [4 ,5 ]
Isobe, Ken-ichi [1 ]
Suzuki, Haruhiko [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Immunol, Nagoya, Aichi 4668550, Japan
[2] Brawijaya Univ, Fac Sci, Dept Biol, Malang 65145, East Java, Indonesia
[3] Nagoya Univ, Grad Sch Med, Dept Occupat & Environm Hlth, Nagoya, Aichi 4668550, Japan
[4] Mie Univ, Grad Sch Med, Dept Canc Vaccine, Tsu, Mie 5148507, Japan
[5] Mie Univ, Grad Sch Med, Dept Immunogene Therapy, Tsu, Mie 5148507, Japan
基金
日本学术振兴会;
关键词
in vitro assay; mouse; suppression; Treg;
D O I
10.1093/intimm/dxn052
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD8(+)CD122(+) regulatory T cells (CD8(+)CD122(+) Treg) are naturally occurring Treg that effectively suppress the proliferation and IFN-gamma production of both CD8(+) and CD4(+) target cells. This study investigated the molecular mechanisms of the recognition of target cells by CD8(+)CD122(+) Treg using an in vitro culture system that reconstitutes the regulatory action of these cells. Naive CD8(+)CD122(+) Treg co-cultured with pre-activated T cells became active Treg that produced IL-10 and suppressed IFN-gamma production from the target T cells. CD8(+)CD122(+) Treg effectively suppressed the IFN-gamma production of the target cells of syngeneic mouse strains but not of allogeneic mouse strains with incompatible MHC. By using MHC-congeneic mouse strains, MHC-restricted suppression by CD8(+)CD122(+) Treg was further confirmed. The blockade of cell surface molecules either on the Treg or on the target cells by specific blocking antibodies indicated that H-2K, H-2D, alpha beta TCR and CD8 were involved in the regulatory action but I-A and Qa-1 were not. These results indicate that CD8(+)CD122(+) Treg recognize already-activated T cells via the interaction of conventional MHC class I-alpha beta TCR and become active regulatory cells that produce IL-10 and suppress the target cells.
引用
收藏
页码:937 / 947
页数:11
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