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抗 CC 趋化因子受体 4 抗体 mogamulizumab 治疗成人 T 细胞白血病/淋巴瘤患者时乙型肝炎病毒再激活。

Reactivation of hepatitis B virus in a patient with adult T-cell leukemia-lymphoma receiving the anti-CC chemokine receptor 4 antibody mogamulizumab.

机构信息

Department of Hematology, Imamura Bun-in Hospital, Kagoshima, Japan.

出版信息

Hepatol Res. 2014 Mar;44(3):354-7. doi: 10.1111/hepr.12117. Epub 2013 Apr 18.

Abstract

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.

摘要

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。

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