Human lymphoblastoid interferon therapy in chronic hepatitis B virus carriers.

G J Alexander
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Abstract

alpha-Interferon and beta-interferon have been used therapeutically in chronic hepatitis B virus (HBV) infection for more than a decade. It is now clear that alpha-interferons are an effective therapy for a proportion of chronic HBV carriers. A course of at least three, and possibly as long as 4 months is required at a dose of 5-10 MU three times a week. Those responding to therapy usually develop a marked hepatitis in the second and third months of therapy, which precedes permanent loss of markers of viral replication. In a proportion of patients, not only are HBe antigen and HBV DNA cleared from serum, but HBsAg may also be cleared, albeit over a longer time course; anti-HBs develops in a few of these patients. Although close to being an established form of therapy for chronic HBV infection, the responsive subgroups remain to be defined. Studies over the next few years will be directed at identifying those groups responsive, or not responsive, to alpha-interferons and thereafter seeking other antiviral agents that could be used in combination with alpha-interferon to augment the response rate.

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人淋巴母细胞干扰素治疗慢性乙型肝炎病毒携带者。
α -干扰素和β -干扰素用于治疗慢性乙型肝炎病毒(HBV)感染已有十多年的历史。现在很清楚,干扰素是一种有效的治疗慢性乙肝病毒携带者的比例。一个疗程至少为3个月,可能长达4个月,剂量为5-10毫微克,每周3次。那些对治疗有反应的人通常在治疗的第二和第三个月出现明显的肝炎,这是在病毒复制标志物永久丧失之前。在一定比例的患者中,不仅HBe抗原和HBV DNA从血清中被清除,HBsAg也可能被清除,尽管需要更长的时间;这些患者中有少数会出现抗hbs。虽然接近于慢性HBV感染的既定治疗形式,但反应亚群仍有待确定。未来几年的研究将致力于确定对干扰素有反应或无反应的群体,然后寻找其他可与干扰素联合使用的抗病毒药物,以提高反应率。
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