Will interferon-free regimens prevail?

Will interferon-free regimens prevail?
复制标题

无干扰素治疗方案会流行吗?

DOI:
--
复制
发表时间:
2012
期刊:
影响因子:
29.4
通讯作者:
S. Zeuzem
S. Zeuzem
中科院分区:
医学1区
文献类型:
--
作者:
C. Welsch;S. Zeuzem

文献摘要

参考文献

被引文献

相似文献

许多有前景的针对丙型肝炎病毒(HCV)蛋白的小分子抑制剂(定向抗病毒药物[DAA])和靶向宿主细胞因子的化合物(宿主靶向药物[hta])目前正处于药物开发和临床试验阶段,而基于聚乙二醇干扰素(Peg-IFN)的治疗方法的禁禁症和不良反应限制了其临床适用性。越来越多的替代治疗方案正在推动对节省干扰素方案的研究,并为干扰素在HCV治疗中的未来地位问题铺平道路。美国食品和药物管理局(fda)和欧洲药品管理局(ema)最近批准了2种daa,开启了慢性丙型肝炎病毒感染(CHC)治疗的新时代。新的护理标准是三联治疗,将先前的标准,1 Peg-IFN- +利巴韦林(RBV)与酮酰胺蛋白酶抑制剂相结合。新的护理标准被批准用于感染基因型1型HCV的患者,这是欧洲和北美最流行的基因型。酮酰胺化合物boceprevir (Victrelis, Merck & Co, Whitehouse Station, NJ)和telaprevir (Incivek, Vertex Pharmaceuticals, Cambridge, MA)被设计用于模拟基因型1的天然NS3/4A蛋白酶底物
Many promising small molecule inhibitors directed against hepatitis C virus (HCV) proteins (directacting antiviral [DAA] agents) and compounds targeting host cell factors (host-targeting agents [HTAs]) are currently in the drug development and clinical trial pipeline, whereas contraindications and adverse effects limit the clinical applicability of peginterferon (Peg-IFN)-based therapies. The increasing number of alternative treatment options is driving the investigation of interferon-sparing regimens and paving the way for the question on the future place for interferon in HCV therapy. The recent approval of 2 DAAs by the US Food and Drug Administration and European Medicines Agency has opened a new era in the treatment of chronic HCV infection (CHC). The new standard of care is a triple therapy, combining the previous standard, 1 Peg-IFN- plus ribavirin (RBV), with a ketoamide protease inhibitor. The new standard of care is licensed for patients infected with genotype 1 HCV, the most prevalent genotype in Europe and North America. Ketoamide compounds, boceprevir (Victrelis, Merck & Co, Whitehouse Station, NJ) and telaprevir (Incivek, Vertex Pharmaceuticals, Cambridge, MA), are designed to mimic the natural NS3/4A protease substrate in genotype 1
DOI: 10.1056/nejmoa020047
发表时间: 2002-09-26
影响因子: 158.5
作者:
Fried, MW;Shiffman, ML;Yu, J
通讯作者: Yu, J