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Dendritic Cells Coordinate the Development and Homeostasis of Organ-Specific Regulatory T Cells.

Immunity | 2016

Although antigen recognition mediated by the T cell receptor (TCR) influences many facets of Foxp3(+) regulatory T (Treg) cell biology, including development and function, the cell types that present antigen to Treg cells in vivo remain largely undefined. By tracking a clonal population of Aire-dependent, prostate-specific Treg cells in mice, we demonstrated an essential role for dendritic cells (DCs) in regulating organ-specific Treg cell biology. We have shown that the thymic development of prostate-specific Treg cells required antigen presentation by DCs. Moreover, Batf3-dependent CD8α(+) DCs were dispensable for the development of this clonotype and had negligible impact on the polyclonal Treg cell repertoire. In the periphery, CCR7-dependent migratory DCs coordinated the activation of organ-specific Treg cells in the prostate-draining lymph nodes. Our results demonstrate that the development and peripheral regulation of organ-specific Treg cells are dependent on antigen presentation by DCs, implicating DCs as key mediators of organ-specific immune tolerance.

Pubmed ID: 27037189 RIS Download

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: R01 AI110507
  • Agency: NCI NIH HHS, United States
    Id: CA183357
  • Agency: NIAID NIH HHS, United States
    Id: T32 AI007090
  • Agency: NCI NIH HHS, United States
    Id: T32 CA009594
  • Agency: NCI NIH HHS, United States
    Id: P30 CA008748
  • Agency: NIAID NIH HHS, United States
    Id: R01AI110507
  • Agency: NCI NIH HHS, United States
    Id: R01 CA166770
  • Agency: NCI NIH HHS, United States
    Id: R01CA166770
  • Agency: NCI NIH HHS, United States
    Id: R01CA160371
  • Agency: NCI NIH HHS, United States
    Id: R01 CA160371
  • Agency: NCI NIH HHS, United States
    Id: F31 CA183357

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