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Human-induced pluripotent stem cells derived hematopoietic progenitor cells for treatment of hematopoietic failure among trauma hemorrhagic shock patients

机译:人源性多能干细胞来源的造血祖细胞用于治疗创伤性失血性休克患者的造血功能衰竭

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摘要

Hematopoietic failure (HF) has been observed in trauma hemorrhagic shock (T/HS) patients. Multiple factors are involved. Elevated serum levels of cytokines, catecholamine, granulocyte colony stimulating factor, peripheral blood hematopoietic progenitor cells (HPCs) and decreased expression of erythropoietin receptor are associated with HF among T/HS. HF leads to anaemia, susceptibility to infection, sepsis and multi-organ failure. There is a lack of molecular understanding of HF and its potential therapeutic strategies. Cell-based therapy has ability to modulate the production of inflammatory cytokines, vascular dysfunction, tissue damage and apoptosis. Human-induced pluripotent stem cells (iPSC) derived HPCs may have the ability to restore HF in T/HS. Autologous cell-based iPSC have great promises for various diseases such as Alzheimer's disease, Parkinson's disease, cardiovascular disease, diabetes, amyotrophic lateral sclerosis, and spinal cord injury without ethical concerns. Similarly, treatment with iPSC derived hematopoietic stem cells can used for the treatment of HF among T/HS and may also improve the outcome. Here, we review the potential of human iPSC derived HSC to reversed HF following T/HS.
机译:在创伤性失血性休克(T / HS)患者中观察到造血功能衰竭(HF)。涉及多个因素。 T / HS患者的HF与血清细胞因子,儿茶酚胺,粒细胞集落刺激因子,外周血造血祖细胞(HPC)水平升高和促红细胞生成素受体表达降低有关。 HF导致贫血,易感染,败血症和多器官衰竭。缺乏对HF及其潜在治疗策略的分子理解。基于细胞的疗法具有调节炎性细胞因子,血管功能障碍,组织损伤和细胞凋亡的能力。人类诱导的多能干细胞(iPSC)衍生的HPC可能具有在T / HS中恢复HF的能力。基于自体细胞的iPSC对于各种疾病具有广阔的前景,例如阿尔茨海默氏病,帕金森氏病,心血管疾病,糖尿病,肌萎缩性侧索硬化症和脊髓损伤,而无需出于道德考虑。同样,用iPSC衍生的造血干细胞治疗可用于治疗T / HS中的HF,也可改善预后。在这里,我们回顾了人类iPSC衍生的HSC在T / HS后逆转HF的潜力。

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