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α干扰素治疗儿童慢性乙型肝炎的前瞻性随机对照试验

Prospective, randomized controlled trial of interferon-alpha in children with chronic hepatitis B.

作者信息

Ruiz-Moreno M, Rua M J, Molina J, Moraleda G, Moreno A, García-Aguado J, Carreño V

机构信息

Department of Pediatrics, Fundación Jiménez Díaz, Madrid, Spain.

出版信息

Hepatology. 1991 Jun;13(6):1035-9.

PMID:2050319
Abstract

Thirty-six children with chronic hepatitis B were entered into a randomized controlled trial of recombinant human interferon-alpha. All patients had hepatitis B virus DNA and increased levels of aminotransferases in serum for at least 1 yr. Twelve children received 10 MU of interferon-alpha 2b/m2 body surface area three times a week (group I); 12 children received 5 MU/m2 under the same conditions (group II); and 12 children served as controls (group III). During 6 mo of therapy, 12 of 24 (50%) treated patients (7 from group I, 58%, and 5 from group II, 42%) and 2 of 12 (17%) controls lost hepatitis B virus DNA from serum and subsequently remained negative. Comparison of the rate of response in group I vs. controls showed a statistically significant difference (p less than 0.05). Eleven of 12 (92%) treated patients who cleared hepatitis B virus DNA from serum lost HBeAg, seroconverted to anti-HBe and had improvement in liver histological findings with loss of hepatitis B virus DNA from liver. In 10, serum ALT levels became normal. Interferon-alpha was well tolerated and all children finished therapy. These findings indicate that a 6-mo course of interferon-alpha is effective in inducing a serological, biochemical and histological remission of disease in approximately 50% of children with chronic hepatitis B.

摘要

36名慢性乙型肝炎患儿参与了重组人α干扰素的随机对照试验。所有患儿血清中乙肝病毒DNA及转氨酶水平升高至少1年。12名患儿每周3次接受10 MUα干扰素2b/m²体表面积治疗(I组);12名患儿在相同条件下接受5 MU/m²治疗(II组);12名患儿作为对照(III组)。在6个月的治疗期间,24名接受治疗的患儿中有12名(50%)(I组7名,占58%;II组5名,占42%)以及12名对照中有2名(17%)血清中乙肝病毒DNA转阴并持续呈阴性。I组与对照组的应答率比较显示出统计学上的显著差异(p<0.05)。血清中乙肝病毒DNA转阴的12名接受治疗的患儿中有11名(92%)HBeAg消失,血清转换为抗-HBe,肝脏组织学表现改善,肝脏中乙肝病毒DNA消失。其中10名患儿血清ALT水平恢复正常。α干扰素耐受性良好,所有患儿均完成治疗。这些结果表明,6个月疗程的α干扰素对约50%的慢性乙型肝炎患儿有效,可诱导疾病的血清学、生化及组织学缓解。

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