T regulatory and primed uncommitted CD4 T cells express CD73, which suppresses effector CD4 T cells by converting 5′-adenosine monophosphate to adenosine

JJ Kobie, PR Shah, L Yang, JA Rebhahn… - The Journal of …, 2006 - journals.aai.org
JJ Kobie, PR Shah, L Yang, JA Rebhahn, DJ Fowell, TR Mosmann
The Journal of Immunology, 2006journals.aai.org
Abstract CD73 (5′-ectonucleotidase) is expressed by two distinct mouse CD4 T cell
populations: CD25+(FoxP3+) T regulatory (Treg) cells that suppress T cell proliferation but
do not secrete IL-2, and CD25− uncommitted primed precursor Th (Thpp) cells that secrete
IL-2 but do not suppress in standard Treg suppressor assays. CD73 on both Treg and Thpp
cells converted extracellular 5′-AMP to adenosine. Adenosine suppressed proliferation
and cytokine secretion of Th1 and Th2 effector cells, even when target cells were activated …
Abstract
CD73 (5′-ectonucleotidase) is expressed by two distinct mouse CD4 T cell populations: CD25+(FoxP3+) T regulatory (Treg) cells that suppress T cell proliferation but do not secrete IL-2, and CD25− uncommitted primed precursor Th (Thpp) cells that secrete IL-2 but do not suppress in standard Treg suppressor assays. CD73 on both Treg and Thpp cells converted extracellular 5′-AMP to adenosine. Adenosine suppressed proliferation and cytokine secretion of Th1 and Th2 effector cells, even when target cells were activated by anti-CD3 and anti-CD28. This represents an additional suppressive mechanism of Treg cells and a previously unrecognized suppressive activity of Thpp cells. Infiltration of either Treg or Thpp cells at inflammatory sites could potentially convert 5′-AMP generated by neutrophils or dying cells into the anti-inflammatory mediator adenosine, thus dampening excessive immune reactions.
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