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      NK cells mediate reduction of GVHD by inhibiting activated, alloreactive T cells while retaining GVT effects.

      Blood
      Animals, Apoptosis, Bone Marrow Transplantation, CD4-Positive T-Lymphocytes, immunology, CD8-Positive T-Lymphocytes, Cytokines, biosynthesis, Fas Ligand Protein, deficiency, genetics, Female, Graft vs Host Disease, prevention & control, Graft vs Tumor Effect, Inflammation Mediators, metabolism, Interferon-gamma, Interleukin-2 Receptor alpha Subunit, Killer Cells, Natural, transplantation, Lymphocyte Activation, Male, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Pore Forming Cytotoxic Proteins, T-Lymphocytes, cytology, T-Lymphocytes, Regulatory, Transplantation, Homologous

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          Abstract

          Natural killer (NK) cells suppress graft-versus-host disease (GVHD) without causing GVHD themselves. Our previous studies demonstrated that allogeneic T cells and NK cells traffic similarly after allogeneic bone marrow transplantation (BMT). We therefore investigated the impact of donor NK cells on donor alloreactive T cells in GVHD induction. Animals receiving donor NK and T cells showed improved survival and decreased GVHD score compared with controls receiving donor T cells alone. Donor T cells exhibited less proliferation, lower CD25 expression, and decreased interferon-gamma (IFN-gamma) production in the presence of NK cells. In vivo, we observed perforin- and Fas ligand (FasL)-mediated reduction of donor T cell proliferation and increased T cell apoptosis in the presence of NK cells. Further, activated NK cells mediated direct lysis of reisolated GVHD-inducing T cells in vitro. The graft-versus-tumor (GVT) effect was retained in the presence of donor NK cells. We demonstrate a novel mechanism of NK cell-mediated GVHD reduction whereby donor NK cells inhibit and lyse autologous donor T cells activated during the initiation of GVHD.

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