| Literature DB >> 27037189 |
Daniel S Leventhal1, Dana C Gilmore1, Julian M Berger1, Saki Nishi1, Victoria Lee1, Sven Malchow1, Douglas E Kline2, Justin Kline2, Donald J Vander Griend3, Haochu Huang4, Nicholas D Socci5, Peter A Savage6.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27037189 PMCID: PMC4842258 DOI: 10.1016/j.immuni.2016.01.025
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745