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重组人粒细胞集落刺激因子长期应用于肌萎缩侧索硬化症患者的安全性和可行性。

Safety and feasibility of long term administration of recombinant human granulocyte-colony stimulating factor in patients with amyotrophic lateral sclerosis.

作者信息

Grassinger Jochen, Khomenko Andrei, Hart Christina, Baldaranov Dobri, Johannesen Siw W, Mueller Gunnar, Schelker Roland, Schulte-Mattler Wilhelm, Andreesen Reinhard, Bogdahn Ulrich

机构信息

University Hospital Regensburg, Department of Internal Medicine III, Regensburg, Germany.

University Hospital Regensburg, Department of Neurology, Regensburg, Germany.

出版信息

Cytokine. 2014 May;67(1):21-8. doi: 10.1016/j.cyto.2014.02.003. Epub 2014 Feb 26.

Abstract

Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neuronal disease resulting in a loss of the upper and lower motor neurons and subsequent death within three to four years after diagnosis. Mouse models and preliminary human exposure data suggest that the treatment with granulocyte-colony stimulating factor (G-CSF) has neuro-protective effects and may delay ALS progression. As data on long-term administration of G-CSF in patients with normal bone marrow (BM) function are scarce, we initiated a compassionate use program including 6 ALS patients with monthly G-CSF treatment cycles. Here we demonstrate that G-CSF injection was safe and feasible throughout our observation period up to three years. Significant decrease of mobilization efficiency occurred in one patient and a loss of immature erythroid progenitors was observed in all six patients. These data imply that follow-up studies analyzing BM function during long-term G-CSF stimulation are required.

摘要

肌萎缩侧索硬化症(ALS)是一种快速进展的神经元疾病,会导致上下运动神经元丧失,并在诊断后三到四年内死亡。小鼠模型和初步的人体暴露数据表明,使用粒细胞集落刺激因子(G-CSF)进行治疗具有神经保护作用,可能会延缓ALS的进展。由于关于正常骨髓(BM)功能的患者长期使用G-CSF的数据稀缺,我们启动了一项同情用药计划,纳入了6例ALS患者,采用每月一次的G-CSF治疗周期。在此我们证明,在长达三年的观察期内,注射G-CSF是安全可行的。一名患者的动员效率显著下降,所有六名患者均观察到未成熟红细胞祖细胞减少。这些数据表明,需要进行后续研究以分析长期G-CSF刺激期间的BM功能。

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