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Dickkopf-3, an immune modulator in peripheral CD8 T-cell tolerance.

Abstract
In healthy individuals, T cells react against incoming pathogens, but remain tolerant to self-antigens, thereby preventing autoimmune reactions. CD4 regulatory T cells are major contributors in induction and maintenance of peripheral tolerance, but a regulatory role has been also reported for several subsets of CD8 T cells. To determine the molecular basis of peripheral CD8 T-cell tolerance, we exploited a double transgenic mouse model in which CD8 T cells are neonatally tolerized following interaction with a parenchymal self-antigen. These tolerant CD8 T cells have regulatory capacity and can suppress T cells in an antigen-specific manner during adulthood. Dickkopf-3 (DKK3) was found to be expressed in the tolerant CD8 T cells and to be essential for the observed CD8 T-cell tolerance. In vitro, genetic deletion of DKK3 or blocking with antibodies restored CD8 T-cell proliferation and IL-2 production in response to the tolerizing self-antigen. Moreover, exogenous DKK3 reduced CD8 T-cell reactivity. In vivo, abrogation of DKK3 function reversed tolerance, leading to eradication of tumors expressing the target antigen and to rejection of autologous skin grafts. Thus, our findings define DKK3 as a immune modulator with a crucial role for CD8 T-cell tolerance.
AuthorsMaria Papatriantafyllou, Gerhard Moldenhauer, Julia Ludwig, Anna Tafuri, Natalio Garbi, Gorana Hollmann, Günter Küblbeck, Alexandra Klevenz, Sabine Schmitt, Georg Pougialis, Christof Niehrs, Hermann-Josef Gröne, Gunter J Hämmerling, Bernd Arnold, Thilo Oelert
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 109 Issue 5 Pg. 1631-6 (Jan 31 2012) ISSN: 1091-6490 [Electronic] United States
PMID22307622 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adaptor Proteins, Signal Transducing
  • Dkk3 protein, mouse
  • Intercellular Signaling Peptides and Proteins
Topics
  • Adaptor Proteins, Signal Transducing
  • Animals
  • Blotting, Western
  • CD8-Positive T-Lymphocytes (cytology, immunology)
  • Cell Proliferation
  • Cytotoxicity, Immunologic
  • Flow Cytometry
  • Immune Tolerance (physiology)
  • Intercellular Signaling Peptides and Proteins (physiology)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction

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