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膦甲酸钠治疗慢性乙型肝炎病毒E抗原携带者

Foscarnet therapy in chronic hepatitis B virus E antigen carriers.

作者信息

Bain V G, Daniels H M, Chanas A, Alexander G J, Williams R

机构信息

Liver Unit, Kings College Hospital, London, England.

出版信息

J Med Virol. 1989 Oct;29(2):152-5. doi: 10.1002/jmv.1890290214.

Abstract

Foscarnet (trisodium phosphonoformate) is a novel antiviral agent that inhibits viral-specific DNA polymerase. In the present study, eight males with chronic HBV carriage (HBeAg and HBV-DNA seropositivity greater than 12 months) showing chronic persistent hepatitis (CPH) or chronic active hepatitis (CAH) on liver biopsy received either a continuous infusion of foscarnet at 0.15 mg/kg/min for 7 days or 180 mg/kg/day divided into three daily boluses for 2 weeks. In all eight, HBV-DNA levels fell during therapy (median, 401 pg/40 microliters serum; range, 4-3, 100) vs. pretreatment levels (median, 533 pg/40 microliters; range, 30-4, 175), but in none was HBV-DNA undetectable at any stage. Within 1 month, the HBV-DNA had risen to pretreatment levels in all but one patient (with the lowest pretreatment level), who cleared HBeAg and developed anti-HBe within 3 months. Two further patients were anti-HBe positive at 6 months, but their pretreatment serum HBV-DNA levels were already low, suggesting a high probability of spontaneous seroconversion. Toxicity was not evident with the continuous infusion, but for those receiving IV bolus therapy, serum creatinine and phosphate levels rose in three of four patients, necessitating a 25% dose reduction. There was no difference in the effect on serum HBV-DNA between the two regimes. We conclude that foscarnet has only modest antiviral activity in chronic HBV carriers.

摘要

膦甲酸钠(三钠膦酰甲酸盐)是一种新型抗病毒药物,可抑制病毒特异性DNA聚合酶。在本研究中,8名慢性乙肝病毒携带者(HBeAg和HBV-DNA血清阳性超过12个月),肝活检显示为慢性持续性肝炎(CPH)或慢性活动性肝炎(CAH),接受了两种治疗方案:一种是以0.15mg/kg/min的速度持续输注膦甲酸钠7天;另一种是每日180mg/kg,分3次静脉推注,共2周。所有8名患者在治疗期间HBV-DNA水平均下降(中位数,血清401pg/40微升;范围,4-3100),而治疗前水平为(中位数,533pg/40微升;范围,30-4175),但在任何阶段均未检测不到HBV-DNA。在1个月内,除1名患者(治疗前水平最低)外,所有患者的HBV-DNA均回升至治疗前水平,该患者在3个月内清除了HBeAg并产生了抗-HBe。另外2名患者在6个月时抗-HBe呈阳性,但他们治疗前的血清HBV-DNA水平已经很低,提示自发血清学转换的可能性很高。持续输注时毒性不明显,但接受静脉推注治疗的患者中,4名患者中有3名血清肌酐和磷酸盐水平升高,需要减少25%的剂量。两种治疗方案对血清HBV-DNA的影响没有差异。我们得出结论,膦甲酸钠对慢性乙肝病毒携带者只有适度的抗病毒活性。

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