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      Inhibitory feedback loop between tolerogenic dendritic cells and regulatory T cells in transplant tolerance.

      The Journal of Immunology Author Choice
      Animals, Antibodies, Monoclonal, pharmacology, Antigens, CD45, immunology, CD4-Positive T-Lymphocytes, Cell Communication, drug effects, Cells, Cultured, Dendritic Cells, Drug Synergism, Feedback, Guanidines, Heart Transplantation, Immunosuppressive Agents, Lymphocyte Activation, Lymphocyte Culture Test, Mixed, Male, Mice, Mice, Inbred BALB C, Mice, Inbred C3H, Mice, Inbred C57BL, T-Lymphocyte Subsets, Transplantation Tolerance, Transplantation, Heterotopic

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          Abstract

          An active role of T regulatory cells (Treg) and tolerogenic dendritic cells (Tol-DC) is believed important for the induction and maintenance of transplantation tolerance. However, interactions between these cells remain unclear. We induced donor-specific tolerance in a fully MHC-mismatched murine model of cardiac transplantation by simultaneously targeting T cell and DC function using anti-CD45RB mAb and LF 15-0195, a novel analog of the antirejection drug 15-deoxyspergualin, respectively. Increases in splenic Treg and Tol-DC were observed in tolerant recipients as assessed by an increase in CD4(+)CD25(+) T cells and DC with immature phenotype. Both these cell types exerted suppressive effects in MLR. Tol-DC purified from tolerant recipients incubated with naive T cells induced the generation/expansion of CD4(+)CD25(+) Treg. Furthermore, incubation of Treg isolated from tolerant recipients with DC progenitors resulted in the generation of DC with Tol-DC phenotype. Treg and Tol-DC generated in vitro were functional based on their suppressive activity in vitro. These results are consistent with the notion that tolerance induction is associated with a self-maintaining regulatory loop in which Tol-DC induce the generation of Treg from naive T cells and Treg programs the generation of Tol-DC from DC progenitors.

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