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Expansion and Activation Kinetics of Immune Cells during Early Phase of GVHD in Mouse Model Based on Chemotherapy Conditioning

机译:基于化学疗法条件的小鼠模型中GVHD早期免疫细胞的扩增和活化动力学

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In the present paper, we have investigated early pathophysiological events in graft-versus-host disease (GVHD), a major complication to hematopoietic stem cell transplantation (HSCT). BLLB/c female mice conditioned with busulfan/cyclophosphamide (Bu-Cy) were transplanted with allogeneic male C57BL/6. Control group consisted of syngeneic transplanted Balb/c mice. In allogeneic settings, significant expansion and maturation of donor dendritic cells (DCs) were observed at day +3, while donor T-cells CD8+ were increased at day +5 (230%) compared to syngeneic HSCT. Highest levels of inflammatory cytokines IL-2, IFN-gamma, and TNF-alfa at day +5 matched T-cell activation. Concomitantly na?ve T-cells gain effecr-memory phenotype and migrated from spleen to peripheral lymphoid organs. Thus, in the very early phase of GHVD following Bu-Cy conditioning donor, DCs play an important role in the activation of donor T cells. Subsequently, donor na?ve T-cells gain effector-memory phenotype and initiate GVHD.
机译:在本文中,我们研究了移植物抗宿主病(GVHD)的早期病理生理事件,这是造血干细胞移植(HSCT)的主要并发症。将以白消安/环磷酰胺(Bu-Cy)适应的BLLB / c雌性小鼠移植同种异体雄性C57BL / 6。对照组由同基因移植的Balb / c小鼠组成。在同种异体环境中,与同系HSCT相比,在+3天时观察到供体树突状细胞(DC)显着扩增和成熟,而在+5天时供体T细胞CD8 +升高(230%)。在第5天时,最高水平的炎症细胞因子IL-2,IFN-γ和TNF-α与T细胞活化相匹配。幼稚的T细胞随之获得有效的记忆表型,并从脾脏迁移到外周淋巴器官。因此,在BuHV调节供体后GHVD的早期阶段,DC在供体T细胞的活化中起着重要作用。随后,纯天然T细胞获得效应记忆表型并启动GVHD。

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