Department of Hematology, Imamura Bun-in Hospital, Kagoshima, Japan.
Hepatol Res. 2014 Mar;44(3):354-7. doi: 10.1111/hepr.12117. Epub 2013 Apr 18.
The introduction of molecularly targeted drugs has increased the risk of reactivation of hepatitis B virus (HBV), which is a potentially fatal complication following anticancer chemotherapy even in patients who have previously resolved their HBV infection. CC chemokine receptor 4 (CCR4) has been identified as a novel molecular target in antibody therapy for patients with adult T-cell leukemia-lymphoma (ATL) and peripheral T-cell lymphoma, and the humanized anti-CCR4 monoclonal antibody mogamulizumab has been developed. We reported HBV reactivation of an ATL patient with previously resolved HBV infection after mogamulizumab treatment in a dose-finding study for this antibody. Our retrospective analysis using preserved samples also revealed the detailed kinetics of HBV DNA levels before and just after HBV reactivation.
分子靶向药物的引入增加了乙型肝炎病毒(HBV)再激活的风险,即使在先前已清除 HBV 感染的患者中,这也是癌症化疗后潜在致命的并发症。趋化因子受体 4(CCR4)已被确定为成人 T 细胞白血病-淋巴瘤(ATL)和外周 T 细胞淋巴瘤抗体治疗的新型分子靶点,并且已经开发出了人源化抗 CCR4 单克隆抗体 mogamulizumab。我们报道了在这项抗体的剂量发现研究中,一名先前已清除 HBV 感染的 ATL 患者在 mogamulizumab 治疗后发生了 HBV 再激活。我们使用保存样本的回顾性分析还揭示了 HBV 再激活之前和之后 HBV DNA 水平的详细动力学。