E to myocardial structure without perceptible changes in inflammatory infiltration (Fig. 2C, 2D). All these data support that CD4+CD252Nrp1+ T cells synergized with a non-therapeutic dose of Rapamycin to prolong the survival of fully MHC-mismatched cardiac allograft.3. Adoptive transfer of CD4+CD252Nrp1+ T cells changes the intragraft and systemic inflammatory cytokine expressionNext, we examined the impact of CD4+CD252Nrp1+ T cells on the expression of intragraft and serum inflammatory cytokines. To this end, on day 7 after transplantation, cardiac allografts were harvested for qRT-PCR analysis and blood was harvested for ELISA assay. Compared with allografts derived from untreated recipient mice, allografts from both Rapamycin and CD4+CD252Nrp1+ T cells treated recipients showed significantly lower levels of IFN-c and IL-17 expression, and combined therapy of Rapamycin and CD4+CD252Nrp1+ T cells further reduced the intragraft expression of IFN-c and IL-17 (Fig. 3A, 3B). In contrast, administration of Rapamycin together with CD4+CD252Nrp1+ T cells significantly PD-168393 increased the intragraft expression of IL-10, while no discernable difference for expressions were detected in Rapamycin or CD4+CD252Nrp1+ T cells alone treated mice in comparison with untreated control (Fig. 3C). Meanwhile, administration of CD4+CD252Nrp1+ T cells rather than Rapamycin significantly increased the intragraft expression of TGF-b, and combined therapy of Rapamycin 
and CD4+CD252Nrp1+ T cells further increased TGF-b expression (Fig. 3D). We also detected increased expression of Foxp3 and Nrp1 mRNA in the CD4+CD252Nrp1+ T cells but not Rapamycin-only treated recipients. Foxp3 and Nrp1 mRNA levels further increased in the mice treated with the combination of both therapies as compared with the untreated controls. Even though the Rapamycin-only treated mice showed lower Nrp1 mRNA expression within the grafted tissues, almost similar levels of Foxp3 expression2. Adoptive transfer of CD4+CD252Nrp1+ T cells synergize with Rapamycin to prevent allograft rejectionNext we sought to address the in vivo impact of CD4+CD252Nrp1+ T cells on allograft rejection through a fully MHC-mismatched (BALB/cC57BL/6) murine abdominal heterotopic cardiac transplant model. Transplantation of syngeneic grafts (C57BL/6C57BL/6) served as controls. As shown in Fig. 2A, cardiac arrest occurred within one week if no treatment was given. Rapamycin or CD4+CD252Nrp1+ T cells alone prolonged the median survival time 15755315 (MST) to 26 days and 37 days, respectively. Combined therapy of CD4+CD252Nrp1+ T cells and Rapamycin significantly prolonged the MST of cardiac allografts to 75 days, indicating that 
CD4+CD252Nrp1+ T cells synergized with Rapamycin to prevent allograft rejection. To confirm the above results, allografts from each study group were harvested on day 7 post-transplantation and subjected to histological analysis. While grafts from syngeneic transplantation had intact myocardial structure, the most severe inflammatory cell infiltration and destruction of myocardial tissue structure wasFigure 1. CD4+CD252Nrp1+ T cells possess potent order Homotaurine suppressive function in vitro. (A) Freshly isolated CD4+CD252Nrp1+ T cells (105, C57BL/6) were co-cultured with syngeneic responder CD4+CD252 T cells (C57BL/6) in different ratios (0, 1:8, 1:4, 1:2, 1:1) in order to address stimulation induced by irradiated BALB/c (donor) splenocytes (105). Cell proliferation was determined by 3H thymidine incorporation. (B) Cytokine.E to myocardial structure without perceptible changes in inflammatory infiltration (Fig. 2C, 2D). All these data support that CD4+CD252Nrp1+ T cells synergized with a non-therapeutic dose of Rapamycin to prolong the survival of fully MHC-mismatched cardiac allograft.3. Adoptive transfer of CD4+CD252Nrp1+ T cells changes the intragraft and systemic inflammatory cytokine expressionNext, we examined the impact of CD4+CD252Nrp1+ T cells on the expression of intragraft and serum inflammatory cytokines. To this end, on day 7 after transplantation, cardiac allografts were harvested for qRT-PCR analysis and blood was harvested for ELISA assay. Compared with allografts derived from untreated recipient mice, allografts from both Rapamycin and CD4+CD252Nrp1+ T cells treated recipients showed significantly lower levels of IFN-c and IL-17 expression, and combined therapy of Rapamycin and CD4+CD252Nrp1+ T cells further reduced the intragraft expression of IFN-c and IL-17 (Fig. 3A, 3B). In contrast, administration of Rapamycin together with CD4+CD252Nrp1+ T cells significantly increased the intragraft expression of IL-10, while no discernable difference for expressions were detected in Rapamycin or CD4+CD252Nrp1+ T cells alone treated mice in comparison with untreated control (Fig. 3C). Meanwhile, administration of CD4+CD252Nrp1+ T cells rather than Rapamycin significantly increased the intragraft expression of TGF-b, and combined therapy of Rapamycin and CD4+CD252Nrp1+ T cells further increased TGF-b expression (Fig. 3D). We also detected increased expression of Foxp3 and Nrp1 mRNA in the CD4+CD252Nrp1+ T cells but not Rapamycin-only treated recipients. Foxp3 and Nrp1 mRNA levels further increased in the mice treated with the combination of both therapies as compared with the untreated controls. Even though the Rapamycin-only treated mice showed lower Nrp1 mRNA expression within the grafted tissues, almost similar levels of Foxp3 expression2. Adoptive transfer of CD4+CD252Nrp1+ T cells synergize with Rapamycin to prevent allograft rejectionNext we sought to address the in vivo impact of CD4+CD252Nrp1+ T cells on allograft rejection through a fully MHC-mismatched (BALB/cC57BL/6) murine abdominal heterotopic cardiac transplant model. Transplantation of syngeneic grafts (C57BL/6C57BL/6) served as controls. As shown in Fig. 2A, cardiac arrest occurred within one week if no treatment was given. Rapamycin or CD4+CD252Nrp1+ T cells alone prolonged the median survival time 15755315 (MST) to 26 days and 37 days, respectively. Combined therapy of CD4+CD252Nrp1+ T cells and Rapamycin significantly prolonged the MST of cardiac allografts to 75 days, indicating that CD4+CD252Nrp1+ T cells synergized with Rapamycin to prevent allograft rejection. To confirm the above results, allografts from each study group were harvested on day 7 post-transplantation and subjected to histological analysis. While grafts from syngeneic transplantation had intact myocardial structure, the most severe inflammatory cell infiltration and destruction of myocardial tissue structure wasFigure 1. CD4+CD252Nrp1+ T cells possess potent suppressive function in vitro. (A) Freshly isolated CD4+CD252Nrp1+ T cells (105, C57BL/6) were co-cultured with syngeneic responder CD4+CD252 T cells (C57BL/6) in different ratios (0, 1:8, 1:4, 1:2, 1:1) in order to address stimulation induced by irradiated BALB/c (donor) splenocytes (105). Cell proliferation was determined by 3H thymidine incorporation. (B) Cytokine.
