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基于粒细胞集落刺激因子和促红细胞生成素的细胞疗法:心肌梗死血管生成的一种有前景的策略。

G-CSF- and erythropoietin-based cell therapy: a promising strategy for angiomyogenesis in myocardial infarction.

作者信息

Kang Hyun-Jae, Kim Hyo-Soo

机构信息

Innovative Research Institute for Cell Therapy, Department of Internal Medicine, Seoul National University Hospital, 28 Yongun-Dong, Chongno-Gu, Seoul, 110-744, South Korea.

出版信息

Expert Rev Cardiovasc Ther. 2008 Jun;6(5):703-13. doi: 10.1586/14779072.6.5.703.

Abstract

Granulocyte colony-stimulating factor (G-CSF) and erythropoietin are two cytokines that have been demonstrated to improve cardiac function and perfusion in myocardial infarction. G-CSF was initially evaluated as a stem cell mobilizer and erythropoietin as a cytoprotective agent. However, both cytokines have direct cytoprotective effects and stem cell-mobilizing ability. Direct cytoprotective effects of both cytokines are commonly mediated by the Jak-STAT pathway. In preclinical study, G-CSF and erythropoietin improved cardiac function and perfusion by angiomyogenesis and protection of cardiomyocytes in myocardial infarction. However, results from recent clinical trials did not support beneficial effects of cytokine therapy with G-CSF or erythropoietin alone in patients with myocardial infarction. Further studies are required to elucidate the mechanism of action and to improve therapeutic efficacy by employing novel strategies, such as combined cytokines.

摘要

粒细胞集落刺激因子(G-CSF)和促红细胞生成素是两种已被证明可改善心肌梗死患者心脏功能和灌注的细胞因子。G-CSF最初被评估为干细胞动员剂,促红细胞生成素则被评估为细胞保护剂。然而,这两种细胞因子都具有直接的细胞保护作用和干细胞动员能力。这两种细胞因子的直接细胞保护作用通常由Jak-STAT信号通路介导。在临床前研究中,G-CSF和促红细胞生成素通过血管生成和保护心肌梗死中的心肌细胞来改善心脏功能和灌注。然而,最近的临床试验结果并不支持单独使用G-CSF或促红细胞生成素进行细胞因子治疗对心肌梗死患者有益。需要进一步研究以阐明其作用机制,并通过采用联合细胞因子等新策略来提高治疗效果。

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