在具有不同HBV血清模式的个体中使用双重ART
Thomas Swaine1, Sanjay Bhagani1,2
1Department of HIV Medicine, Royal Free London NHS Trust.
Current opinion in HIV and AIDS
|January 14, 2026
概括
治疗艾滋病毒的两种药物方案 (2DR) 减少了药物负担,但需要仔细查乙型肝炎 (HBV). 切换到2DRs具有较低的HBV再激活风险,特别是含有拉米武丁的选择.
科学领域:
- 传染性疾病 传染性疾病
- 肝病学 肝病学是一种肝病学.
- 抗逆转录病毒疗法是一种治疗方法.
背景情况:
- 两种药物方案 (2DR) 越来越多地被推用于艾滋病毒治疗,以尽量减少药物负担和毒性.
- 在2DR中排除了诺福维尔和拉米武丁/emtricitabine,这引发了人们对乙型肝炎病毒 (HBV) 获取和重新激活的担忧.
研究的目的:
- 审查2DRs对艾滋病毒感染者的HBV获取和重新激活的影响.
- 评估与不同2DR配方相关的HBV再激活风险.
主要方法:
- 对病例系列,队列研究和随机对照试验的系统审查,评估2DRs患者的HBV结局.
- 基于特定药物组合和先前的HBV暴露 (HBsAg阳性) 的HBV再激活 (HBVr) 风险的分析.
主要成果:
- 在切换到含有拉米武丁的2DR时,HBVr的风险是可以忽略不计的.
- 转换为诺福维尔和拉米武丁/埃姆特里西塔宾无治疗的患者的整体HBVr风险较低 (~1%).
- 即使是远程的HBsAg阳性也显著增加了HBVr.的风险.
结论:
- 切换前的HBV血清学评估对于HIV感染者启动2DRs至关重要.
- 对于没有先前暴露或没有HBsAb的个人,建议接种HBV疫苗.
- 建议进行仔细的监测和患者咨询,特别是关于含有拉米武丁的2DRs的低HBVr风险.
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