Nestvold Janne M, Omdal Bente K, Dai Ke-Zheng, Martens Anton, Benestad Haakon B, Vaage John T, Rolstad Bent
Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, and Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway.
Transplantation. 2008 Jan 15;85(1):102-11. doi: 10.1097/01.tp.0000296856.53493.1f.
We have employed a rat model for human acute myeloid leukemia, a promyelocytic leukemia in the BN rat strain (BNML), to develop new protocols for immunotherapy in combination with allogeneic bone marrow transplantation (alloBMT). The status of mixed chimerism in allotransplanted rats provided an opportunity for immunotherapy using alloreactive donor cells. In addition to T or natural killer (NK) cells, we introduced a second infusion of bone marrow cells as prophylactic donor lymphocyte infusions (DLI) to test whether an effective graft-versus-leukemia (GVL) response could be obtained without clinical graft-versus-host disease (GVHD).
BN rats were sublethally irradiated and transplanted with T-cell depleted bone marrow cells from either fully major histocompatibility complex (MHC)-mismatched (PVG) donor rats or MHC-matched (PVG.1N) as controls. Seven days after transplantation, rats were given 500 leukemic cells to mimic minimal residual disease. Additional cellular therapy was given at day +7. The efficiency of DLI was monitored by chimerism analysis in peripheral blood.
Rats receiving infusions of NK cells succumbed to leukemia. T-DLI induced complete donor T-cell chimerism and lethal GVHD. A second alloBMT protected against leukemia. This effect was dependent on an MHC incompatibility between the donor and host and also on the presence of alloreactive T cells in the second bone marrow inoculum, resulting in an increased, mixed donor T-cell chimerism.
A second prophylactic transplantation influenced the degree of T-cell chimerism to balance favorably between GVL and GVHD. If applicable to humans, repeated alloBMT may provide a novel approach to leukemia therapy.
我们采用了一种人类急性髓系白血病大鼠模型,即BN大鼠品系中的早幼粒细胞白血病(BNML),来开发与异基因骨髓移植(alloBMT)联合的免疫治疗新方案。同种异体移植大鼠中混合嵌合体的状态为使用同种反应性供体细胞进行免疫治疗提供了机会。除了T细胞或自然杀伤(NK)细胞外,我们还进行了第二次骨髓细胞输注作为预防性供体淋巴细胞输注(DLI),以测试是否可以在无临床移植物抗宿主病(GVHD)的情况下获得有效的移植物抗白血病(GVL)反应。
对BN大鼠进行亚致死剂量照射,并移植来自完全主要组织相容性复合体(MHC)不匹配(PVG)供体大鼠或MHC匹配(PVG.1N)作为对照的T细胞去除的骨髓细胞。移植后7天,给大鼠注射500个白血病细胞以模拟微小残留病。在第7天给予额外的细胞治疗。通过外周血嵌合体分析监测DLI的效率。
接受NK细胞输注的大鼠死于白血病。T-DLI诱导了完全的供体T细胞嵌合体和致死性GVHD。第二次alloBMT可预防白血病。这种效应取决于供体和宿主之间的MHC不相容性,也取决于第二次骨髓接种物中同种反应性T细胞的存在,导致混合供体T细胞嵌合体增加。
第二次预防性移植影响了T细胞嵌合体的程度,从而在GVL和GVHD之间实现了有利的平衡。如果适用于人类,重复alloBMT可能为白血病治疗提供一种新方法。