| Literature DB >> 23758811 |
M B Ezzelarab1, A F Zahorchak, L Lu, A E Morelli, G Chalasani, A J Demetris, F G Lakkis, M Wijkstrom, N Murase, A Humar, R Shapiro, D K C Cooper, A W Thomson.
Abstract
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. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: Costimulation blockade; dendritic cells; memory T cells; rapamycin; renal transplant; rhesus macaques
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Year: 2013 PMID: 23758811 PMCID: PMC4070451 DOI: 10.1111/ajt.12310
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086