Department of Surgery, Starzl Transplantation Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Am J Transplant. 2013 Aug;13(8):1989-2005. doi: 10.1111/ajt.12310. Epub 2013 Jun 11.
We examined the influence of regulatory dendritic cells (DCreg), generated from cytokine-mobilized donor blood monocytes in vitamin D3 and IL-10, on renal allograft survival in a clinically relevant rhesus macaque model. DCreg expressed low MHC class II and costimulatory molecules, but comparatively high levels of programmed death ligand-1 (B7-H1), and were resistant to pro-inflammatory cytokine-induced maturation. They were infused intravenously (3.5-10 × 10(6) /kg), together with the B7-CD28 costimulation blocking agent CTLA4Ig, 7 days before renal transplantation. CTLA4Ig was given for up to 8 weeks and rapamycin, started on Day -2, was maintained with tapering of blood levels until full withdrawal at 6 months. Median graft survival time was 39.5 days in control monkeys (no DC infusion; n = 6) and 113.5 days (p < 0.05) in DCreg-treated animals (n = 6). No adverse events were associated with DCreg infusion, and there was no evidence of induction of host sensitization based on circulating donor-specific alloantibody levels. Immunologic monitoring also revealed regulation of donor-reactive memory CD95(+) T cells and reduced memory/regulatory T cell ratios in DCreg-treated monkeys compared with controls. Termination allograft histology showed moderate combined T cell- and Ab-mediated rejection in both groups. These findings justify further preclinical evaluation of DCreg therapy and their therapeutic potential in organ transplantation.
我们研究了在一个临床相关的恒河猴模型中,从细胞因子动员的供体血液单核细胞中生成的调节性树突状细胞(DCreg)对肾移植存活的影响,这些细胞在维生素 D3 和 IL-10 中生成。DCreg 表达低水平的 MHC Ⅱ类和共刺激分子,但高水平的程序性死亡配体-1(B7-H1),并且对促炎细胞因子诱导的成熟具有抗性。它们在肾移植前 7 天静脉内输注(3.5-10×10^6/kg),同时输注 B7-CD28 共刺激阻断剂 CTLA4Ig。CTLA4Ig 最多给予 8 周,雷帕霉素在第 -2 天开始,通过降低血液水平逐渐停药,直到 6 个月完全停药。在对照组猴子(无 DC 输注;n=6)中,中位移植物存活时间为 39.5 天,而在 DCreg 治疗组动物(n=6)中为 113.5 天(p<0.05)。DCreg 输注没有不良事件发生,并且根据循环供体特异性同种抗体水平,没有证据表明诱导宿主致敏。免疫监测还显示,与对照组相比,DCreg 治疗的猴子中,供体反应性记忆 CD95(+)T 细胞得到调节,记忆/调节性 T 细胞比值降低。终止移植物组织学显示两组均存在中度联合 T 细胞和 Ab 介导的排斥反应。这些发现证明了 DCreg 治疗在器官移植中的进一步临床前评估及其治疗潜力。