Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
Ann N Y Acad Sci. 2013 Jul;1291:69-76. doi: 10.1111/nyas.12218.
The identification of hepatitis C virus (HCV) as the causative agent of non-A and non-B hepatitis, over 20 years ago, fueled an intensive effort to develop direct-acting antivirals targeting the viral polymerase and protease, two key proteins critical for HCV replication. However, it took more than two decades for these efforts to be realized with boceprevir, one of the two HCV protease inhibitors approved for treatment of HCV infection in 2011. The development of boceprevir is a major advancement in the ability to treat HCV infection and a significant step toward the long-term goal of eradicating chronic HCV infection. Both as a first-in-class agent and an entirely new modality for treating HCV infection, many challenges were encountered during the discovery and development of this compound. The lessons learned in overcoming these obstacles offer insights and pave the way for the newly emerging field of HCV antiviral therapeutics. This paper will describe the discovery and development of a first-in-class direct antiviral treatment for chronic hepatitis C infection, boceprevir, marketed around the world as Victrelis™.
20 多年前,丙型肝炎病毒 (HCV) 被确定为非甲非乙型肝炎的病原体,这促使人们积极研发针对病毒聚合酶和蛋白酶的直接作用抗病毒药物,这两种关键蛋白对 HCV 的复制至关重要。然而,这些努力直到 2011 年批准的两种 HCV 蛋白酶抑制剂之一博赛泼维(boceprevir)的出现才得以实现。博赛泼维的开发是治疗 HCV 感染能力的重大进步,也是朝着根除慢性 HCV 感染这一长期目标迈出的重要一步。作为首个同类药物和治疗 HCV 感染的全新模式,在发现和开发该化合物的过程中遇到了许多挑战。在克服这些障碍的过程中吸取的经验教训为新兴的 HCV 抗病毒治疗领域提供了见解和启示。本文将介绍首个用于慢性丙型肝炎感染的同类直接抗病毒治疗药物博赛泼维(boceprevir)的发现和开发,该药在全球以 VictrelisTM 的商品名销售。