The

control mice were treated with BM and CY only. Donor skin grafts survived longer than 100 days in chimeric mice but were rejected shortly in control CY-treated mice (mean ± SD = 12 ± 3 days, Fig. 1D). Skin grafts from third-party control C3H (H-2k) mice were used to determined if chimeric KU-57788 datasheet mice corroborate donor-specific tolerance. Skin grafts from C3H mice were rejected shortly in chimeric mice (Fig. 1D, mean ± SD = 11 ± 2 days), suggesting that antigen-specific tolerance was established in the animals with mixed chimerism. The major drawback for BM transplantation is donor T cell-mediated GVHD. Previous studies have demonstrated that adoptive transfer of donor DN Treg cells can inhibit CD8+ T cell-mediated autoimmunity and GVHD [[27, 28]]. To determine if adoptive transfer of DN Treg cells play a role in GVHD in the current model, we put it to test by comparison with CD4+ TAM Receptor inhibitor or CD8+ T cells. C57BL/6 CD4+ T cells or CD8+ T cells purified from BM donor C57BL/6 mice were i.v. injected to BALB/c mice (4 × 106/mouse) on day 0. All mice received CY and BM transplantation as the DN Treg-cell treatment described in Fig. 1. As shown in Fig. 2A and B, all mice that received DN

Treg cells survived beyond 100 days without a decrease in body weight or signs of GVHD. Pathology analysis showed that hepatocytes, liver cell cords, and portal and venous structures were normal with no evidence of GVHD (Fig. 2C). In contrast, the mice that received CD4+ or CD8+ T cells developed GVHD with weight loss and mortality (Fig. 2A and B). Infiltrating mononuclear cells, proliferation in bile ducts, and abnormal portal and venous structure, and typical lesions of chronic GVHD were evident (Fig. 2C). Hence, these data indicate that adoptive transfer CD4+ or CD8+ T cells, but not DN Treg cells, induces GVHD in our protocol. T cells play a major role in BM graft rejection [[29, 30]]. Our data indicate that DN Treg cells in combination with immunosuppression can help AZD9291 donor BM transplantation

and establish-mixed chimerism (Fig. 1). We are interested in determining the mechanism of T-cell suppression in our protocol. We tested the effect of adoptive transfer of DN Treg cells on various clones of T cells bearing different T-cell receptors (TCRs). To focus on the effect on T cells, we depleted NK cells in recipients. BALB/c mice (n = 3) were treated by intraperitoneal (i.p.) injection of NK-cell depletion antibody (anti-Asialo, GM1) on day −4 and −1. Recipient BALB/c mice were treated with cyclophosphamide (200 mg/kg, i.p.) on day 0 and 3. Donor C57BL/6 DN Treg cells (107) were injected into BALB/c mice at same day, while mice of control group were treated with PBS. Recipient mice lymph node cells were harvested on day 8, stained with TCR Vβ antibodies, each combined with anti-CD4 antibody, and anti-CD8 antibody before flow cytometry analysis.