Therapeutic effects of non-preconditioning allogeneic hematopoietic stem cell transplantation on acute radiation injury

Q1 Health Professions
Liren Qian, Yu Liu, Xiaoxuan Lu, Jiaxin Liu
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Abstract

Objective

To investigate the therapeutic effects of non-preconditioning allogeneic hematopoietic stem cell transplantation (allo-HSCT) on acute radiation injury.

Methods

Irradiated mice were randomly divided into six groups, i.e., the control group, the irradiation group, and groups treated with transplantation at 0, 4, 8, and 12 ​d post-irradiation, with 10 mice in each group. The survival rates, graft versus host disease (GvHD), and chimerism of the mice in various groups were assessed.

Results

The maximum 60 ​d survival rate of mice treated with non-preconditioning allo-HSCT at 0, 4, and 8 ​d after 6.5 ​Gy radiation increased to 70% and 80%, respectively, significantly higher than that of mice that did not undergo non-preconditioning allo-HSCT (50%; P < 0.05). The survival rate of mice undergoing non-preconditioning allo-HSCT at 12 ​d after radiation no longer significantly decreased. No pronounced GvHD was observed in the mice. The mice treated with non-preconditioning allo-HSCT at 0, 4, 8, and 12 ​d post-radiation exhibited chimerism rates of 80.53%, 92.75%, 80.46%, and 80.87%, respectively, at 56 ​d post-transplantation. At 28 ​d after non-preconditioning allo-HSCT, the donor-derived fluorescent cells in recipient mice increased significantly (P ​< ​0.05).

Conclusions

This study will fill the gap in the field of radiation medicine and hematopoietic stem cell transplantation (HSCT) by addressing challenges that hinder the application of traditional HSCT, such as donor shortage, toxicity of preconditioning chemotherapy, the occurrence of GvHD, and the administration of post-transplantation immunosuppressants. The results would provide theoretical value and application prospects for research on radiation medicine and HSCT.
非预处理异基因造血干细胞移植治疗急性辐射损伤的疗效观察
目的探讨非预处理异基因造血干细胞移植对急性放射损伤的治疗作用。方法将辐照小鼠随机分为6组,即对照组、辐照组和放疗后0、4、8、12 d的移植治疗组,每组10只。观察各组小鼠的存活率、移植物抗宿主病(GvHD)和嵌合性。结果在6.5 Gy辐照后0、4、8 d,非预处理同种异体造血干细胞移植小鼠的最大60 d存活率分别提高到70%和80%,显著高于未进行非预处理同种异体造血干细胞移植的小鼠(50%;P & lt;0.05)。在放疗后12 d进行非预处理的同种异体造血干细胞移植的小鼠存活率不再显著下降。小鼠未见明显的GvHD。在放射后0、4、8和12 d进行非预处理的小鼠,在移植后56 d嵌合率分别为80.53%、92.75%、80.46%和80.87%。非预处理同种异体造血干细胞移植后28 d,受体小鼠供体来源的荧光细胞显著增加(P <;0.05)。结论本研究将填补放射医学和造血干细胞移植(HSCT)领域的空白,解决阻碍传统HSCT应用的挑战,如供体短缺、预处理化疗的毒性、GvHD的发生以及移植后免疫抑制剂的使用。研究结果对放射医学和HSCT的研究具有一定的理论价值和应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Radiation Medicine and Protection
Radiation Medicine and Protection Health Professions-Emergency Medical Services
CiteScore
2.10
自引率
0.00%
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0
审稿时长
103 days
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