Steptoe R J, Fu F, Li W, Drakes M L, Lu L, Demetris A J, Qian S, McKenna H J, Thomson A W
Thomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, PA 15213, USA.
J Immunol. 1997 Dec 1;159(11):5483-91.
Treatment of mice with the recently cloned hemopoietic growth factor Flt3 ligand (FL; 10 microg/day for 10 days) resulted in a large increase in myeloid lineage cells within the liver. While the number of nonparenchymal cells (NPC) harvested from liver increased about 9-fold, a 90-fold increase was observed in the proportion of CD11c+ dendritic cells (DC) recovered from NPC following overnight (18-h) culture in granulocyte-macrophage CSF. In contrast, only a 50% increase was seen in CD11c+ cells within heart single cell suspensions and in the number of DC obtained from hearts after 18-h culture. Liver NPC and heart cell suspensions freshly isolated from 10-day FL-treated animals exhibited increased T cell allostimulatory capacity compared with controls. Overnight cultured DC from livers of FL-treated animals expressed both higher levels of costimulatory molecules (CD80 and CD86) and allostimulatory activity than those from controls. Heart-derived DC also displayed enhanced stimulatory capacity. Pretreatment of organ donors with FL for either 5 or 10 days before transplant of organs to normal recipients abrogated the spontaneous liver allograft acceptance normally observed and resulted in delayed or acute graft rejection (median survival times, 40 and 12 days, respectively). Heart rejection was significantly accelerated by pretreatment of donors with FL for 5 or 10 days (median survival times, 8 and 7 days, respectively, vs 12 days in controls). These novel findings reveal the potent immunologic adjuvant properties of FL in vivo. They also show that substantial augmentation of the number of potential allostimulatory cells in donor organs before transplantation favors rejection rather than tolerance induction.
用最近克隆的造血生长因子Flt3配体(FL;每天10微克,共10天)处理小鼠,导致肝脏内髓系细胞大量增加。虽然从肝脏收获的非实质细胞(NPC)数量增加了约9倍,但在粒细胞-巨噬细胞集落刺激因子中过夜(18小时)培养后,从NPC中回收的CD11c+树突状细胞(DC)比例增加了90倍。相比之下,心脏单细胞悬液中的CD11c+细胞以及18小时培养后从心脏获得的DC数量仅增加了50%。与对照组相比,从接受10天FL处理的动物新鲜分离的肝脏NPC和心脏细胞悬液表现出增强的T细胞同种异体刺激能力。来自FL处理动物肝脏的过夜培养DC表达的共刺激分子(CD80和CD86)水平更高,且同种异体刺激活性也高于对照组。心脏来源的DC也表现出增强的刺激能力。在将器官移植给正常受体之前,用FL对器官供体进行5天或10天的预处理,消除了通常观察到的肝脏同种异体移植的自发接受,并导致延迟或急性移植排斥(中位存活时间分别为40天和12天)。用FL对供体进行5天或10天的预处理可显著加速心脏排斥反应(中位存活时间分别为8天和7天,而对照组为12天)。这些新发现揭示了FL在体内具有强大的免疫佐剂特性。它们还表明,移植前供体器官中潜在同种异体刺激细胞数量的大量增加有利于排斥反应而非诱导耐受。