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本文引用的文献

1
Treatment of Anemia With Darbepoetin Prior to Dialysis Initiation and Clinical Outcomes: Analyses From the Trial to Reduce Cardiovascular Events With Aranesp Therapy (TREAT).在开始透析前使用达贝泊汀治疗贫血和临床结局:来自用阿法依泊汀治疗降低心血管事件试验(TREAT)的分析。
Am J Kidney Dis. 2019 Mar;73(3):309-315. doi: 10.1053/j.ajkd.2018.10.006. Epub 2018 Dec 19.
2
Long-term maintenance of hemoglobin levels in hemodialysis patients treated with bi-weekly epoetin beta pegol switched from darbepoetin alfa: a single-center, 12-month observational study in Japan.接受每两周一次的聚乙二醇化促红细胞生成素β治疗的血液透析患者血红蛋白水平的长期维持,从阿法达贝泊汀转换而来:日本一项单中心、为期12个月的观察性研究。
J Artif Organs. 2019 Jun;22(2):146-153. doi: 10.1007/s10047-018-1080-z. Epub 2018 Nov 14.
3
Comparing Therapeutic Efficacy and Safety of Epoetin Beta and Epoetin Alfa in the Treatment of Anemia in End-Stage Renal Disease Hemodialysis Patients.比较β型促红细胞生成素和α型促红细胞生成素治疗终末期肾病血液透析患者贫血的疗效和安全性。
Am J Nephrol. 2018;48(4):251-259. doi: 10.1159/000493097. Epub 2018 Sep 25.
4
Erythropoietin enhances migration of human neuroblastoma cells: in vitro studies and potential therapeutic implications.促红细胞生成素增强人神经母细胞瘤细胞的迁移:体外研究及潜在治疗意义。
J Cancer Stem Cell Res. 2017;5. Epub 2017 Apr 27.
5
Update on Anemia in ESRD and Earlier Stages of CKD: Core Curriculum 2018.慢性肾脏病早期和终末期肾病贫血更新:2018 年核心课程。
Am J Kidney Dis. 2018 Mar;71(3):423-435. doi: 10.1053/j.ajkd.2017.09.026. Epub 2018 Jan 11.
6
rhEPO Enhances Cellular Anti-oxidant Capacity to Protect Long-Term Cultured Aging Primary Nerve Cells.重组人促红细胞生成素增强细胞抗氧化能力以保护长期培养的衰老原代神经细胞。
J Mol Neurosci. 2017 Aug;62(3-4):291-303. doi: 10.1007/s12031-017-0937-6. Epub 2017 Jun 21.
7
Methoxy Polyethylene Glycol-Epoetin Beta as a Novel Erythropoiesis Stimulating Agent with Possible Nephroprotective and Cardiovascular Protective Effects in Non-Dialysis Chronic Kidney Disease Patients.甲氧基聚乙二醇-促红细胞生成素β作为一种新型促红细胞生成刺激剂,对非透析慢性肾脏病患者可能具有肾脏保护和心血管保护作用。
Curr Pharm Biotechnol. 2017;18(4):303-308. doi: 10.2174/1389201018666170127104801.
8
Erythropoiesis stimulating agents and reno-protection: a meta-analysis.促红细胞生成素与肾脏保护:一项荟萃分析
BMC Nephrol. 2017 Jan 11;18(1):14. doi: 10.1186/s12882-017-0438-4.
9
Peginesatide for the treatment of anemia due to chronic kidney disease - an unfulfilled promise.聚乙二醇化促红细胞生成素用于治疗慢性肾脏病所致贫血——一个未实现的承诺。
Expert Opin Drug Saf. 2016 Oct;15(10):1421-6. doi: 10.1080/14740338.2016.1218467. Epub 2016 Aug 23.
10
Association between responsiveness to methoxy polyethylene glycol-epoetin beta and renal survival in patients with non-dialysis-dependent chronic kidney disease: A pooled analysis of individual patient-level data from clinical trials.非透析依赖性慢性肾脏病患者对聚乙二醇化促红细胞生成素β的反应性与肾脏生存之间的关联:来自临床试验个体患者水平数据的汇总分析
Nephrology (Carlton). 2017 Oct;22(10):769-775. doi: 10.1111/nep.12842.

新型促红细胞生成剂的进展:临床与分子方法

Updates on Novel Erythropoiesis-Stimulating Agents: Clinical and Molecular Approach.

作者信息

Moradi Zahra, Maali Amirhosein, Shad Javad Sadeghi, Farasat Alireza, Kouchaki Reza, Moghadami Mona, Ahmadi Mohamad Hosein, Azad Mehdi

机构信息

1Student Research Committee, Iran University of Medical Sciences, Tehran, Iran.

2Student Research Committee, Babol University of Medical Sciences, Babol, Iran.

出版信息

Indian J Hematol Blood Transfus. 2020 Jan;36(1):26-36. doi: 10.1007/s12288-019-01170-1. Epub 2019 Sep 16.

DOI:10.1007/s12288-019-01170-1
PMID:32174689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7042474/
Abstract

Erythropoietin (EPO) is an important hormone responsible for the stimulation of hematopoiesis which is impaired in a variety of diseases, such as chronic kidney disease, cancer chemotherapy, and the use of some anti-HIV drugs. Difficulties in the purification of endogenous EPO due to problems such as technical limitations, heterogeneity of target cells, inadequate amount and immunogenicity of the resultant product, had limited the entry of endogenous EPO in the clinical applications. The integration of medical biotechnology and hematology has introduced novel procedures for the production of human recombinant erythropoietin (rHuEPO), and other erythropoiesis-stimulating agents (ESAs). To investigate and produce rHuEPO, the first step is to recognize the molecular biology and functional pathways, structure, metabolism, and basic physiology of EPO. In this review, all clinical indications, side effects, challenges and notable points regarding EPO, rHuEPO, and other ESAs have also been addressed along with its molecular characterization, such as the modifications needed to optimize their rHuEPO biosynthesis.

摘要

促红细胞生成素(EPO)是一种重要的激素,负责刺激造血作用,而造血作用在多种疾病中会受到损害,如慢性肾病、癌症化疗以及某些抗艾滋病毒药物的使用。由于技术限制、靶细胞异质性、所得产物量不足和免疫原性等问题,内源性EPO的纯化存在困难,这限制了内源性EPO在临床应用中的使用。医学生物技术与血液学的结合引入了生产人重组促红细胞生成素(rHuEPO)和其他促红细胞生成刺激剂(ESA)的新方法。为了研究和生产rHuEPO,第一步是了解EPO的分子生物学、功能途径、结构、代谢和基本生理学。在这篇综述中,还讨论了关于EPO、rHuEPO和其他ESA的所有临床适应症、副作用、挑战和要点,以及它们的分子特征,如优化rHuEPO生物合成所需的修饰。