Adenosine generation catalyzed by CD39 and CD73 expressed on regulatory T cells mediates immune suppression.
作者信息
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, Robson Simon C
机构信息
Department of Medicine, Harvard Medical School, Transplantation Research Center, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
出版信息
J Exp Med. 2007 Jun 11;204(6):1257-65. doi: 10.1084/jem.20062512. Epub 2007 May 14.
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 ectoenzymes generate 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.