Trivella Juan Pablo, Gutierrez Julio, Martin Paul
University of Miami/Jackson Memorial Hospital, Department of Gastroenterology and Hepatology , 1500 NW 12 Ave, Jackson Medical Tower E-1101, Miami, Fl 33136 , USA.
Expert Opin Pharmacother. 2015 Mar;16(4):617-24. doi: 10.1517/14656566.2015.1012493. Epub 2015 Feb 9.
Treatment of hepatitis C virus (HCV) infection with direct-acting antivirals (DAAs) has revolutionized the care of infected patients. Among these novel compounds are non-nucleoside analogs, which bind viral RNA-dependent RNA polymerase resulting in a conformational change inhibiting RNA synthesis.
Efficacy and tolerability of treatment regimens containing the non-nucleoside analog polymerase inhibitor dasabuvir (ABT-333).
Dasabuvir-containing regimens achieve high rates of sustained virologic response in HCV genotype 1a and 1b-infected patients when combined with other DAAs, namely paritaprevir (ABT-450), ritonavir and ombitasvir (ABT-267). In the populations studied, dasabuvir seems to be well tolerated and safe. The major limitations of this novel drug are its genotype-restricted activity, the necessity to include ribavirin for HCV genotype 1a and the emergence of resistance if not combined with other DDAs.
使用直接作用抗病毒药物(DAA)治疗丙型肝炎病毒(HCV)感染彻底改变了对感染患者的治疗方式。这些新型化合物中有非核苷类似物,它们与病毒RNA依赖性RNA聚合酶结合,导致构象变化,从而抑制RNA合成。
含有非核苷类似物聚合酶抑制剂达沙布韦(ABT - 333)的治疗方案的疗效和耐受性。
当与其他DAA(即帕利瑞韦(ABT - 450)、利托那韦和奥比他韦(ABT - 267))联合使用时,含达沙布韦的治疗方案在HCV 1a和1b基因型感染患者中实现了高持续病毒学应答率。在所研究的人群中,达沙布韦似乎耐受性良好且安全。这种新型药物的主要局限性在于其基因型限制活性、对于HCV 1a基因型需要联合使用利巴韦林以及如果不与其他DAA联合使用会出现耐药性。