Departments of Paediatrics and Pathology, University of Michigan, Ann Arbor, Michigan, USA.
Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Haemophilia. 2022 May;28 Suppl 4(Suppl 4):44-52. doi: 10.1111/hae.14545.
The first wave of gene therapies for haemophilia submitted for regulatory review utilize a liver-directed approach in which a functional gene copy of factor VIII (FVIII) or factor IX (FIX) is packaged inside a recombinant adeno-associated viral vector (rAAV). Following a single treatment event, these particles are taken up into liver cells, where the rAAV uncoats and delivers the DNA to the nucleus of the cell, where genetic elements that accompany the gene allow for efficient expression and secretion of FVIII or FIX protein into the plasma. An immune response to the vector capsid has been manifest by elevations in common liver enzymes that must be diligently followed postinfusion for weeks and months afterward and if signs of toxicity appear, will trigger a course of immunosuppression. Despite this, the studies have shown that this works in the great majority of individuals and the immunosuppression course is either avoided or short-lived for many. Optimal outcomes in the haemophilia population will be dependent on proper screening assessment and maintenance of liver health prior to consideration of gene therapy, close short-term follow up and implementation of immunomodulatory strategies to identify and manage liver toxicity and preserve durable transgene expression. This review proposes best practices to assist clinical teams with overcoming the challenges this platform of therapy poses to the traditional clinical care models and infrastructure within the haemophilia treatment centres (HTCs) who will be coordinating the patient's journey through this potentially transformative therapy.
首批提交监管审查的血友病基因治疗药物采用了肝靶向方法,即将功能正常的凝血因子 VIII (FVIII) 或凝血因子 IX (FIX) 基因拷贝包装在重组腺相关病毒载体 (rAAV) 中。单次治疗后,这些颗粒被肝细胞摄取,rAAV 脱壳并将 DNA 递送至细胞核,伴随基因的遗传元件允许 FVIII 或 FIX 蛋白高效表达和分泌到血浆中。载体衣壳的免疫反应表现为常见肝酶的升高,必须在输注后数周到数月内密切随访,如果出现毒性迹象,将引发免疫抑制治疗。尽管如此,这些研究表明,这种方法在绝大多数个体中都有效,而且许多个体可以避免或短暂接受免疫抑制治疗。在考虑基因治疗之前,对血友病患者进行适当的筛选评估和肝脏健康维护,密切的短期随访以及实施免疫调节策略以识别和管理肝脏毒性并保持持久的转基因表达,将是该治疗方案取得最佳效果的关键。本文提出了最佳实践建议,以帮助临床团队克服该治疗平台给血友病治疗中心 (HTC) 传统临床护理模式和基础设施带来的挑战,这些中心将协调患者接受这种潜在变革性治疗的全过程。