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附加聚乙二醇干扰素可导致 HBeAg 阴性慢性乙型肝炎患者 HBsAg 丢失,这些患者的 HBV DNA 已被长期核苷酸类似物完全抑制。

Add-on peg-interferon leads to loss of HBsAg in patients with HBeAg-negative chronic hepatitis and HBV DNA fully suppressed by long-term nucleotide analogs.

机构信息

Institut Arnault Tzanck, St Laurent du Var, France.

出版信息

J Clin Virol. 2013 Dec;58(4):713-7. doi: 10.1016/j.jcv.2013.09.020. Epub 2013 Sep 29.

Abstract

BACKGROUND AND OBJECTIVE

The aim of this study was to prospectively evaluate whether the addition of peg-IFN to a stable NA regimen leads to loss of HBsAg in HBeAg-negative patients with chronic hepatitis and HBV DNA fully suppressed by long-term NA treatment.

STUDY DESIGN

We analyzed HBsAg levels in 10 HBsAg-positive, HBeAg-negative patients who received peg-IFN alpha-2a in addition to a NA regimen. Treatment lasted a maximum of 96 weeks, according to changes in the HBsAg titer. Before peg-IFN therapy, HBV DNA levels had been below the limit of detection for at least three years.

RESULTS

HBsAg levels declined in nine patients. Among these nine, four became HBsAg-negative after 48 weeks of peg-IFN treatment; these patients received peg-IFN for only 48 weeks. NAs were stopped in these four patients, and these levels remained stable for at least 18 months (loss of HBsAg; HBV-DNA negative). HBs seroconversion was observed in two patients. The remaining five patients received 96 weeks of peg-IFN therapy. One patient became HBsAg-negative at the end of peg-IFN therapy; another became HBsAg-negative six months later. Three patients did not become HBsAg-negative. NAs were stopped in the two patients who became HBsAg-negative with no relapse during 12 months of follow up.

CONCLUSIONS

In HBsAg-positive, HBeAg-negative patients with HBV DNA were fully suppressed by long-term NA treatment, the addition of peg-INF for a maximum of 96 weeks based on HBsAg-titer monitoring led to a loss of HBsAg and cessation of NA therapy in six out of ten patients, with no relapse for 12-18 months of follow up. HBs seroconversion was observed in two patients.

摘要

背景与目的

本研究旨在前瞻性评估聚乙二醇干扰素(peg-IFN)加用在长期核苷(酸)类似物(NA)治疗已实现 HBV DNA 完全抑制、HBeAg 阴性的慢性乙型肝炎患者中是否导致 HBsAg 丢失。

研究设计

我们分析了 10 例 HBsAg 阳性、HBeAg 阴性患者在加用 NA 方案的基础上加用 peg-IFNα-2a 的 HBsAg 水平。根据 HBsAg 滴度变化,治疗时间最长为 96 周。在 peg-IFN 治疗前,HBV DNA 水平已低于检测下限至少 3 年。

结果

9 例患者的 HBsAg 水平下降。其中 4 例在接受 peg-IFN 治疗 48 周后 HBsAg 转阴,这些患者仅接受了 48 周的 peg-IFN 治疗;NA 停药,这些患者至少 18 个月 HBsAg 保持稳定(HBsAg 丢失;HBV-DNA 阴性)。2 例患者出现 HBs 血清学转换。其余 5 例患者接受了 96 周 peg-IFN 治疗。1 例患者在 peg-IFN 治疗结束时 HBsAg 转阴,另 1 例在 6 个月后 HBsAg 转阴。3 例患者未发生 HBsAg 丢失。2 例 HBsAg 转阴的患者在 12 个月的随访中无复发而停用 NA。

结论

在 HBV DNA 长期 NA 治疗已完全抑制的 HBsAg 阳性、HBeAg 阴性患者中,基于 HBsAg 滴度监测,加用 peg-IFN 最多 96 周可导致 10 例患者中的 6 例 HBsAg 丢失和 NA 停药,12-18 个月的随访中无复发。2 例患者出现 HBs 血清学转换。

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