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Blood, 1 January 2008, Vol. 111, No. 1, pp. 251-259.
Prepublished online as a Blood First Edition Paper on October 1, 2007; DOI 10.1182/blood-2007-03-081646.
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IMMUNOBIOLOGY
A2A receptor signaling promotes peripheral tolerance by inducing T-cell anergy and the generation of adaptive regulatory T cells
Paul E. Zarek1,
Ching-Tai Huang2,
Eric R. Lutz3,
Jeanne Kowalski4,
Maureen R. Horton5,
Joel Linden6,
Charles G. Drake3, and
Jonathan D. Powell1,3
1 Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD;
2 Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan;
3 Department of Oncology, Sidney Kimmel Comprehensive Cancer Center,
4 Department of Oncology Biostatistics, and
5 Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD; and
6 Department of Medicine, University of Virginia, Charlottesville, VA
Tissue-derived adenosine, acting via the adenosine A2A receptor (A2AR), is emerging as an important negative regulator of T-cell function. In this report, we demonstrate that A2AR stimulation not only inhibits the generation of adaptive effector T cells but also promotes the induction of adaptive regulatory T cells. In vitro, antigen recognition in the setting of A2AR engagement induces T-cell anergy, even in the presence of costimulation. T cells initially stimulated in the presence of an A2AR agonist fail to proliferate and produce interleukin-2 and interferon (IFN)- when rechallenged in the absence of A2AR stimulation. Likewise, in an in vivo model of autoimmunity, tissue-derived adenosine promotes anergy and abrogates tissue destruction. Indeed, A2AR stimulation inhibits interleukin-6 expression while enhancing the production of transforming growth factor-β. Accordingly, treating mice with A2AR agonists not only inhibits Th1 and Th17 effector cell generation but also promotes the generation of Foxp3+ and LAG-3+ regulatory T cells. In this regard, A2AR agonists fail to prevent autoimmunity by LAG-3–/– clonotypic T cells, implicating an important role for LAG-3 in adenosine-mediated peripheral tolerance. Overall, our findings demonstrate that extracellular adenosine stimulates the A2AR to promote long-term T-cell anergy and the generation of adaptive regulatory T cells.

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