Publication | Open Access
T Regulatory and Primed Uncommitted CD4 T Cells Express CD73, Which Suppresses Effector CD4 T Cells by Converting 5′-Adenosine Monophosphate to Adenosine
449
Citations
56
References
2006
Year
Anti-inflammatory Mediator AdenosineT-regulatory CellImmunologyImmune RegulationRegulatory T CellsImmunologic MechanismCd4 T Cell ResponsesImmunotherapyInflammationT RegulatoryCell SignalingRegulatory T Cell BiologyAutoimmune DiseaseSelf-toleranceT Cell ImmunityAutoimmunityTolerance InductionTreg CellsCell BiologyT Cell BiologyCytokineSignal TransductionCellular Immune ResponseThpp Cells5′-Adenosine MonophosphateMedicineCell Development
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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