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PLoS Biol ; 8(2): e1000302, 2010 Feb 02.
Article in English | MEDLINE | ID: mdl-20126379

ABSTRACT

Immunotherapy using regulatory T cells (Treg) has been proposed, yet cellular and molecular mechanisms of human Tregs remain incompletely characterized. Here, we demonstrate that human Tregs promote the generation of myeloid dendritic cells (DC) with reduced capacity to stimulate effector T cell responses. In a model of xenogeneic graft-versus-host disease (GVHD), allogeneic human DC conditioned with Tregs suppressed human T cell activation and completely abrogated posttransplant lethality. Tregs induced programmed death ligand-1 (PD-L1) expression on Treg-conditioned DC; subsequently, Treg-conditioned DC induced PD-L1 expression in vivo on effector T cells. PD-L1 blockade reversed Treg-conditioned DC function in vitro and in vivo, thereby demonstrating that human Tregs can promote immune suppression via DC modulation through PD-L1 up-regulation. This identification of a human Treg downstream cellular effector (DC) and molecular mechanism (PD-L1) will facilitate the rational design of clinical trials to modulate alloreactivity.


Subject(s)
Antigens, CD/immunology , Dendritic Cells/immunology , Immune Tolerance/immunology , T-Lymphocytes, Regulatory/immunology , Animals , B7-H1 Antigen , Cells, Cultured , Female , Flow Cytometry , Graft vs Host Disease/immunology , Humans , Lymphocyte Activation/immunology , Mice , Signal Transduction/immunology
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