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乙型血友病治疗的最新进展。

Recent advances in hemophilia B therapy.

作者信息

Horava Sarena D, Peppas Nicholas A

机构信息

McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.

Institute for Biomaterials, Drug Delivery, and Regenerative Medicine, The University of Texas at Austin, Austin, TX, USA.

出版信息

Drug Deliv Transl Res. 2017 Jun;7(3):359-371. doi: 10.1007/s13346-017-0365-8.

Abstract

Hemophilia B is a hereditary bleeding disorder caused by the deficiency in coagulation factor IX. Understanding coagulation and the role of factor IX as well as patient population and diagnosis are all critical factors in developing treatment strategies and regimens for hemophilia B patients. Current treatment options rely on protein replacement therapy by intravenous injection, which have markedly improved patient lifespan and quality of life. However, issues with current options include lack of patient compliance due to needle-based administration, high expenses, and potential other complications (e.g., surgical procedures, inhibitor formation). As a result, these treatment options are also limited to developed countries. Recent advantages in hemophilia B treatment have focused on addressing these pain points. Emerging commercial products based on modified factor IX aim to reduce injection frequency. Exploratory research efforts have focused on novel drug delivery systems for orally administered treatment and gene therapy as a potential cure. Such alternative treatment methods are promising options for hemophilia B patients worldwide.

摘要

乙型血友病是一种由凝血因子IX缺乏引起的遗传性出血性疾病。了解凝血过程、因子IX的作用以及患者群体和诊断方法,都是制定乙型血友病患者治疗策略和方案的关键因素。目前的治疗选择依赖于静脉注射蛋白质替代疗法,这显著提高了患者的寿命和生活质量。然而,当前治疗方案存在一些问题,包括基于针头给药导致患者依从性差、费用高昂以及可能出现的其他并发症(如手术、抑制剂形成)。因此,这些治疗方案也仅限于发达国家。乙型血友病治疗的最新进展集中在解决这些痛点上。基于改良因子IX的新兴商业产品旨在减少注射频率。探索性研究工作集中在用于口服治疗的新型药物递送系统和作为潜在治愈方法的基因治疗上。此类替代治疗方法对于全球的乙型血友病患者来说是很有前景的选择。

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