慢性丙型肝炎患者干扰素治疗后循环丙型肝炎病毒迅速减少。

H Saitoh, S Naitoh, H Okamoto, Y Akahane
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引用次数: 5

摘要

慢性丙型肝炎患者采用干扰素(IFN)治疗,并随访血清中丙型肝炎病毒(HCV) RNA和抗HCV抗体。这种反应与血清HCV RNA水平的降低以及HCV基因型和肝脏组织病理学相关。通过停用干扰素6个月后HCV RNA清除率和转氨酶水平正常化来评估干扰素对35例基因型II/1b HCV感染患者的反应,其中11例(31%),18例基因型III/2a患者中13例(72%),6例基因型IV/2b患者中2例(33%);1例基因型为I/1a的患者有应答,而1例基因型为II/1b和IV/2b的双重感染患者无应答。14例慢性持续性肝炎患者中有10例(71%)出现缓解,36例慢性活动性2A肝炎患者中有14例(39%)出现缓解,11例2B肝炎患者中有3例(27%)出现缓解。预处理HCV RNA水平高的患者比预处理水平低的患者获得应答的几率要低。HCV RNA在IFN开始后一天急剧下降,并在2周内持续下降,无论对IFN或HCV基因型的反应如何。相反,抗- hcv下降更为缓慢,且仅在对IFN有反应的患者中。这些结果支持IFN介导的HCV抗病毒作用的快速发展,并支持IFN的治疗作用依赖于肝脏组织病理学以及HCV RNA滴度和基因型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prompt decrease of circulating hepatitis C virus in patients with chronic hepatitis C after treatment with interferon.
Patients with chronic hepatitis C were treated with interferon (IFN) and followed for hepatitis C virus (HCV) RNA and antibody to HCV (anti-HCV) in serum. The response was correlated with decrease in serum levels of HCV RNA, as well as HCV genotypes and liver histopathology. Response to IFN, estimated by clearance of HCV RNA and normalization of aminotransferase levels at 6 months after the withdrawal of IFN, was observed in 11 (31%) of 35 patients infected with HCV of genotype II/1b, 13 (72%) of 18 with genotype III/2a, and 2 (33%) of 6 with genotype IV/2b; a single patient with genotype I/1a responded while the one doubly infected with HCV of genotypes II/1b and IV/2b did not. Response was seen in 10 (71%) of 14 patients with chronic persistent hepatitis, 14 (39%) of 36 with chronic active hepatitis 2A, and 3 (27%) of 11 with 2B. Response was achieved less often in patients with high than low pretreatment levels of HCV RNA. HCV RNA dropped sharply on a day after the start of IFN, and continued to decrease during the 2 weeks, irrespective of the response to IFN or HCV genotypes. In contrast, anti-HCV decreased more gradually and only in responders to IFN. These results support the rapid development of an IFN-mediated antiviral effect on HCV, and support therapeutic effects of IFN dependent on histopathology of liver as well as HCV RNA titers and genotypes.
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