Adenosine generation catalyzed by CD39 and CD73 expressed on regulatory T cells mediates immune suppression

被引:1841
作者
Deaglio, Silvia
Dwyer, Karen M.
Gao, Wenda
Friedman, David
Usheva, Anny
Erat, Anna
Chen, Jiang-Fan
Enjyoji, Keiichii
Linden, Joel
Oukka, Mohamed
Kuchroo, Vijay K.
Strom, Terry B. [1 ]
Robson, Simon C.
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Beth Israel Med Ctr, Sch Med, Transplantat Res Ctr,Dept Surg, Boston, MA 02215 USA
[3] Boston Univ, Med Ctr, Boston, MA 02118 USA
[4] Univ Virginia, Dept Med, Charlottesville, VA 22908 USA
[5] Brigham & Womens Hosp, Ctr Neurol Dis, Dept Neurol, Boston, MA 02115 USA
关键词
D O I
10.1084/jem.20062512
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The study of T regulatory cells (T reg cells) has been limited by the lack of specific surface markers and an inability to define mechanisms of suppression. We show that the expression of CD39/ENTPD1 in concert with CD73/ecto-5'-nucleotidase distinguishes CD4(+)/CD25(+)/ Foxp3(+) T reg cells from other T cells. These ectoenzymesgenerate pericellular adenosine from extracellular nucleotides. The coordinated expression of CD39/CD73 on T reg cells and the adenosine A2A receptor on activated T effector cells generates immunosuppressive loops, indicating roles in the inhibitory function of T reg cells. Consequently, T reg cells from Cd39-null mice show impaired suppressive properties in vitro and fail to block allograft rejection in vivo. We conclude that CD39 and CD73 are surface markers of T reg cells that impart a specific biochemical signature characterized by adenosine generation that has functional relevance for cellular immunoregulation.
引用
收藏
页码:1257 / 1265
页数:9
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