Medical Clinic 2/Institute of Transfusion Medicine and Immunohaematology, University Hospital Frankfurt, Germany.
Department of Hepatology, Queen Mary University of London, United Kingdom.
J Thromb Haemost. 2023 Feb;21(2):200-203. doi: 10.1016/j.jtha.2022.11.026. Epub 2022 Dec 22.
Adeno-associated virus-based gene therapies hemophilia allow long-term transgene expression with reduced annual bleeding rates. Various liver-related aspects are involved in the different phases of gene therapy, such as assessment of liver health in the pretherapy period, patient selection and follow-up, maintenance of liver health after gene therapy, and management of potential short- and long-term adverse events. Increase in alanine aminotransferease is a common adverse event that requires rapid evaluation and an immunosuppressive approach. It is therefore important that hemophilia treaters and hepatologists collaborate at all stages of gene therapy to assess potential safety issues and ensure the long-term success of gene therapy. Special attention should be given to patients with not well-defined conditions, e.g. patients with some degree of liver fibrosis or fatty liver disease, patients with a history of hepatitis C and hepatitis B infection, patients with HIV infection, and patients taking medications that may affect liver function.
腺相关病毒为基础的基因治疗血友病允许长期转基因表达,减少每年出血率。各种与肝脏相关的方面都涉及到基因治疗的不同阶段,如在治疗前评估肝脏健康,患者选择和随访,基因治疗后维持肝脏健康,以及管理潜在的短期和长期不良事件。丙氨酸氨基转移酶升高是一种常见的不良事件,需要快速评估和免疫抑制治疗。因此,血友病治疗者和肝病学家在基因治疗的所有阶段合作,评估潜在的安全问题,并确保基因治疗的长期成功是很重要的。特别关注那些情况不明确的患者,例如有一定程度肝纤维化或脂肪肝疾病的患者,有丙型肝炎和乙型肝炎感染史的患者,感染 HIV 的患者,以及服用可能影响肝功能的药物的患者。