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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Radiation protocols determine acute graft-versus-host disease incidence after allogeneic bone marrow transplantation in murine models.
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Radiation protocols determine acute graft-versus-host disease incidence after allogeneic bone marrow transplantation in murine models.

机译:放射方案确定了小鼠模型中同种异体骨髓移植后的急性移植物抗宿主病发病率。

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PURPOSE: Effects of radiation sources used for total body irradiation (TBI) on Graft-versus-Host Disease (GvHD) induction were examined. MATERIALS AND METHODS: In a T cell receptor (TCR) transgenic mouse model, single fraction TBI was performed with different radiation devices ((60)Coba (137)Cesium; 6 MV linear accelerator), dose rates (0.85; 1.5; 2.9; 5 Gy/min) and total doses before allogeneic bone marrow transplantation (BMT). Recipients were observed for 120 days. Different tissues were examined histologically. RESULTS: Acute GvHD was induced by a dose rate of 0.85 Gy/min ((60)Cobalt) and a total dose of 9 Gy and injection of 5 x 10(5) lymph node cells plus 5 x 10(6) bone marrow cells. Similar results were obtained using 6 MV linear accelerator- (linac-) photons with a dose rate of 1.5 Gy/min and 0.85 Gy/min, a total dose of 9.5 Gy and injection of same cell numbers. TBI with (137)Cesium (dose rate: 2.5 Gy/min) did not lead reproducibly to lethal acute GvHD. CONCLUSIONS: Experimental TBI in murine models may induce different immunological responses, depending on total energy, total single dose and dose rate. GvHD might also be induced by TBI with low dose rates.
机译:目的:检查了用于全身照射(TBI)的辐射源对移植物抗宿主病(GvHD)的诱导作用。材料与方法:在T细胞受体(TCR)转基因小鼠模型中,用不同的辐射装置((60)钴;(137)铯; 6 MV线性加速器),剂量率(0.85; 1.5; 2.9)进行单部分TBI。 ; 5 Gy / min)和异体骨髓移植(BMT)前的总剂量。观察接收者120天。组织学检查不同的组织。结果:急性GvHD的剂量率为0.85 Gy / min((60)Cobalt)和总剂量为9 Gy,并注射5 x 10(5)淋巴结细胞加5 x 10(6)骨髓细胞。使用6个MV线性加速器(linac-)光子以1.5 Gy / min和0.85 Gy / min的剂量率,9.5 Gy的总剂量和注射相同的细胞数获得了相似的结果。含(137)铯的TBI(剂量率:2.5 Gy / min)不能重现致命的急性GvHD。结论:鼠模型中的实验性TBI可能诱导不同的免疫反应,具体取决于总能量,总单剂量和剂量率。低剂量率的TBI也可能诱发GvHD。

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