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三名2/1基因型重组丙型肝炎病毒患者接受直接抗病毒治疗成功。

Successful direct-acting antiviral treatment of three patients with genotype 2/1 recombinant hepatitis C virus.

作者信息

Okada Masako, Hai Hoang, Tamori Akihiro, Uchida-Kobayashi Sawako, Enomoto Masaru, Kumada Hiromitsu, Kawada Norifumi

机构信息

Department of Hepatology, Osaka City University Graduate School of Medicine, 1-4-3 Asahimachi, Abeno-ku, Osaka, 545-8585, Japan.

Department of Hepatology, Toranomon Hospital, Tokyo, Japan.

出版信息

Clin J Gastroenterol. 2019 Jun;12(3):213-217. doi: 10.1007/s12328-018-0922-9. Epub 2018 Nov 16.

Abstract

There have been a few reports on the treatment of patients infected with recombinant hepatitis C virus (HCV) genotype 2/1 strains with direct-acting antivirals (DAAs). We experienced three patients, with genotype 2/1 recombinant HCV, treated with DAAs successfully. The first, a 39-year-old man, was infected with recombinant HCV genotype 2a/1b, a rare variant. The sequence of the relapsed virus showed chimeric HCV 2a/1b with the recombinant breakpoint found at nucleotide +49 from the start of the NS3 region. Sofosbuvir plus ribavirin, a regimen recommended for HCV genotype 2, did not lead to a sustained viral response (SVR). Retreatment with grazoprevir plus elbasvir resulted in an SVR. The second case, a 70-year-old woman, was infected with recombinant HCV genotype 2b/1b. DAA therapy with sofosbuvir plus ledipasvir resulted in an SVR. The third case, a 48-year-old woman, was also infected with recombinant HCV genotype 2b/1b. DAA therapy with daclatasvir plus asunaprevir resulted in an SVR. The baseline sequences of the viruses from both the second and third cases showed chimeric HCV 2b/1b with the recombinant breakpoint found at nucleotide +10 from the NS3 start. We report three cases with 2/1 chimeras and discuss the prevalence and response to therapy.

摘要

关于使用直接作用抗病毒药物(DAA)治疗感染重组丙型肝炎病毒(HCV)2/1基因型毒株患者的报道较少。我们成功治疗了3例感染2/1重组HCV基因型的患者。第一例是一名39岁男性,感染了重组HCV 2a/1b基因型,这是一种罕见的变异体。复发病毒的序列显示为嵌合型HCV 2a/1b,重组断点位于NS3区域起始处核苷酸+49位置。推荐用于HCV基因型2的索磷布韦联合利巴韦林方案未导致持续病毒学应答(SVR)。使用格卡瑞韦联合艾尔巴韦再治疗后获得了SVR。第二例是一名70岁女性,感染了重组HCV 2b/1b基因型。索磷布韦联合来迪派韦的DAA治疗导致了SVR。第三例是一名48岁女性,也感染了重组HCV 2b/1b基因型。达卡他韦联合阿舒瑞韦的DAA治疗导致了SVR。第二例和第三例患者病毒的基线序列均显示为嵌合型HCV 2b/1b,重组断点位于NS3起始处核苷酸+10位置。我们报告3例2/1嵌合体病例,并讨论其流行情况及治疗反应。

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