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淋巴母细胞样α-干扰素每周、每日给药以及与阿昔洛韦联合应用治疗慢性HBeAg阳性肝炎。

Lymphoblastoid alpha-interferon weekly, daily and combined with acyclovir for chronic HBeAg-positive hepatitis.

作者信息

Schalm S W, Heytink R A, Van Buuren H R, De Man R A

出版信息

J Hepatol. 1986;3 Suppl 2:S189-92. doi: 10.1016/s0168-8278(86)80119-2.

DOI:10.1016/s0168-8278(86)80119-2
PMID:3598156
Abstract

Patients with chronic hepatitis B and active viral replication had no change in DNA-polymerase (DNA-p) and HBeAg when treated with weekly injections of lymphoblastoid alpha-interferon (IFN) for 4-10 weeks. Daily IFN (2.5 MU/m2 for a period of 4 weeks) was associated with a significant fall (P less than 0.05) in DNA-p but not in HBeAg; DNA-p remained or became negative in 3 out of 10 patients after stopping therapy. Combination of IFN and intravenous acyclovir (ACV, 15 mg/kg twice daily) led to a significantly greater fall in DNA-p and HBeAg, while tolerance of the combination therapy was excellent. Four out of 5 patients became DNA-p-negative and three HBeAg-negative; subsequently two became HBsAg-negative with anti-HBs. We conclude that weekly IFN appears ineffective. Daily IFN depressed hepatitis B virus replication, but does not change markedly the natural course of the disease. Combination therapy with ACV may be more effective than IFN alone and is well tolerated.

摘要

慢性乙型肝炎且病毒活跃复制的患者,接受每周注射淋巴母细胞α干扰素(IFN)治疗4至10周后,其DNA聚合酶(DNA-p)和HBeAg无变化。每日注射IFN(2.5 MU/m²,持续4周)会使DNA-p显著下降(P<0.05),但HBeAg无变化;10名患者中有3名在停止治疗后DNA-p保持阴性或转为阴性。IFN与静脉注射阿昔洛韦(ACV,15 mg/kg,每日两次)联合使用,可使DNA-p和HBeAg下降幅度显著增大,且联合治疗的耐受性良好。5名患者中有4名DNA-p转为阴性,3名HBeAg转为阴性;随后有2名患者HBsAg转为阴性并产生抗-HBs。我们得出结论,每周注射IFN似乎无效。每日注射IFN可抑制乙型肝炎病毒复制,但不会显著改变疾病的自然病程。ACV联合治疗可能比单独使用IFN更有效,且耐受性良好。

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