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Dual daclatasvir and sofosbuvir for treatment of genotype 3 chronic hepatitis C virus infection

机译:达卡他韦和索非布韦双重用药治疗基因型3型慢性丙型肝炎病毒感染

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摘要

Chronic hepatitis C virus (HCV) infection is one of the most common etiologies of liver-related mortality throughout the world. Traditionally, therapy has been focused on pegylated interferon in combination with ribavirin, with clinical trials demonstrating that HCV genotype 1 had the lowest response rate (40-50%), while genotype 3 had an intermediate response rate (60-70%). Recently, significant advances have been made with all-oral direct-acting antiviral (DAA) therapy, which have significantly improved cure rates for HCV genotype 1. Accordingly, HCV genotype 3 is now potentially the most difficult to treat. One of the most potent DAA medications is sofosbuvir, a pan-genotypic nucleotide analogue that inhibits the NS5B polymerase of HCV. Daclatasvir, a pan-genotypic inhibitor of the HCV NS5A replication complex, was recently approved in the United States for treatment of HCV genotype 3 in conjunction with sofosbuvir. This combination may provide a powerful tool in the treatment of HCV genotype 3.
机译:慢性丙型肝炎病毒(HCV)感染是全世界最常见的与肝脏相关的死亡率的病因之一。传统上,治疗一直集中在聚乙二醇干扰素联合利巴韦林的临床研究中,证明HCV基因型1的响应率最低(40-50%),而基因型3的中度响应率(60-70%)。最近,全口服直接作用抗病毒(DAA)治疗已取得重大进展,已显着提高了HCV基因型1的治愈率。因此,HCV基因型3现在可能是最难治疗的。最有效的DAA药物之一是sofosbuvir,它是一种泛基因型核苷酸类似物,可抑制HCV的NS5B聚合酶。 Daclatasvir是HCV NS5A复制复合物的泛基因型抑制剂,最近在美国被批准与sofosbuvir一起用于治疗HCV基因型3。这种组合可以为治疗HCV基因型3提供强大的工具。

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