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首页> 外文期刊>Bone marrow transplantation >Post transplant persistence of host cells augments the intensity of acute graft-versus-host disease and level of donor chimerism, an explanation for graft-versus-host disease and rapid displacement of host cells seen following non-myeloablative stem
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Post transplant persistence of host cells augments the intensity of acute graft-versus-host disease and level of donor chimerism, an explanation for graft-versus-host disease and rapid displacement of host cells seen following non-myeloablative stem

机译:移植后宿主细胞的持久性增强了急性移植物抗宿主病的强度和供体嵌合水平,这解释了移植物抗宿主病和非清髓性干细胞后宿主细胞的快速移位。

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摘要

Although the use of non-myeloablative stem cell transplantation (NST) reduces the severity of graft-versus-host disease (GVHD), GVHD remains a major complication following allogeneic transplantation. Since following NST in comparison with myeloablative conditioning, higher proportions of host immunohematopoietic cells may persist while donor-derived alloreactive lymphocytes are being infused, thus possibly serving as host antigen presentation for continuous stimulation of donor T cells, we speculated that GVHD may be similarly amplified by conditioning followed by intentional administration of host cells. This hypothesis was tested in a preclinical animal model. Increased incidence of GVHD, higher mortality and increased levels of chimerism were observed in recipients reconstituted with host cells, particularly with non-irradiated spleen cells. Graft-versus-leukemia effect was not impaired by post transplant cell administration. These results suggest that GVHD may be amplified by recipient cell infusion using either irradiated or viable stimulatory host cells, thus possibly explaining in part higher than anticipated incidence of GVHD and rapid displacement of host cells and conversion to 100% donor type cells following NST. Administration of irradiated host antigen-presenting cells post transplantation may thus represent a potential approach for amplification of the alloreactive capacity of donor lymphocytes following stem cell transplantation.
机译:尽管使用非清髓性干细胞移植(NST)可以降低移植物抗宿主病(GVHD)的严重程度,但同种异体移植后GVHD仍然是主要并发症。由于在进行NST后与清髓疗法相比,在注入供体来源的同种异体反应性淋巴细胞的过程中,较高比例的宿主免疫造血细胞可能会持续存在,因此可能用作持续刺激供体T细胞的宿主抗原呈递,因此我们推测GVHD可能会被类似地扩增通过调节,然后有目的地施用宿主细胞。在临床前动物模型中检验了该假设。在用宿主细胞重组的受体中,尤其是在未辐照的脾脏细胞中,观察到了GVHD发生率增加,死亡率更高和嵌合水平升高。移植后施用细胞不会损害移植物抗白血病作用。这些结果表明,GVHD可以通过使用受辐照或可行的刺激性宿主细胞输注受体细胞来扩增,因此可能部分解释了高于预期的GVHD发生率和宿主细胞的快速置换以及NST后转化为100%供体型细胞的情况。移植后给予受辐照的宿主抗原呈递细胞可能是干细胞移植后扩增供体淋巴细胞同种反应能力的潜在方法。

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