Helvaci Mehmet, Kizilgunesler Asli, Kasirga Erhun, Ozbal Ebru, Kuzu Muge, Sozen Gulben
Department of Pediatrics, Social Security Tepecik Teaching Hospital, Izmir, Turkey.
J Gastroenterol Hepatol. 2004 Jul;19(7):785-91. doi: 10.1111/j.1440-1746.2004.03358.x.
Although interferon (IFN) has been approved in the treatment of chronic hepatitis B in children, it is effective only in 30-40% of patients. In some studies it has been suggested that therapeutic use of anti-hepatitis B virus (HBV) vaccine may be beneficial in patients with chronic hepatitis B. The aim of the present study was to compare the efficacy of hepatitis B vaccination and IFN-alpha-2b in combination and IFN-alpha-2b monotherapy in children with chronic hepatitis B.
Fifty treatment-naive children with chronic hepatitis B infection were randomly assigned to receive either 5 million units/m(2) recombinant IFN-alpha-2b subcutaneously three times per week for 9 months, and pre-S2/S vaccine at the beginning and 4 and 24 weeks after initiation of IFN therapy (n = 25) or recombinant IFN-alpha-2b (5 million units/m(2) subcutaneously thrice weekly) alone for 9 months (n = 25). Children were followed for at least 6 months after the end of therapy.
There was no statistically significant difference in the mean alanine aminotransferase levels, histologic activity index and fibrosis scores between combination and IFN monotherapy groups at the end of the therapy and end of the follow-up period. When combination and monotherapy groups were compared, the mean HBV-DNA values were significantly reduced in combination group at the end of the therapy (P = 0.004), but no statistically significant difference was found at the end of the follow up. Sustained HBeAg seroconversion with clearance of HBV-DNA was obtained in 13 of 25 children (52%) treated with combination therapy, and in eight of 25 patients (32%) treated with IFN monotherapy (P = 0.251).
Although the difference was statistically insignificant, the sustained response rates were better in the combination therapy group than in the monotherapy group. The potential benefit of combining IFN and hepatitis B vaccine should be investigated in further studies with different regimens of combination therapy.
尽管干扰素(IFN)已被批准用于治疗儿童慢性乙型肝炎,但仅30%至40%的患者有效。一些研究表明,抗乙型肝炎病毒(HBV)疫苗的治疗性使用可能对慢性乙型肝炎患者有益。本研究的目的是比较乙型肝炎疫苗与干扰素-α-2b联合使用和干扰素-α-2b单药治疗对儿童慢性乙型肝炎的疗效。
50例未接受过治疗的慢性乙型肝炎感染儿童被随机分为两组,一组接受500万单位/m²重组干扰素-α-2b皮下注射,每周3次,共9个月,并在干扰素治疗开始时、第4周和第24周接种前S2/S疫苗(n = 25);另一组仅接受重组干扰素-α-2b(500万单位/m²皮下注射,每周3次),共9个月(n = 25)。治疗结束后,对儿童进行至少6个月的随访。
治疗结束时和随访期末,联合治疗组与干扰素单药治疗组的平均丙氨酸转氨酶水平、组织学活性指数和纤维化评分无统计学显著差异。比较联合治疗组和单药治疗组时,治疗结束时联合治疗组的平均HBV-DNA值显著降低(P = 0.004),但随访期末未发现统计学显著差异。联合治疗的25例儿童中有13例(52%)实现了持续HBeAg血清学转换并清除HBV-DNA,干扰素单药治疗的25例患者中有8例(32%)实现了这一目标(P = 0.251)。
尽管差异无统计学显著性,但联合治疗组的持续缓解率高于单药治疗组。应通过不同联合治疗方案的进一步研究,探讨联合使用干扰素和乙型肝炎疫苗的潜在益处。