Horae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA, USA; Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA.
Pfizer Inc., New York, NY, USA.
Mol Ther. 2022 Apr 6;30(4):1364-1380. doi: 10.1016/j.ymthe.2022.03.004. Epub 2022 Mar 10.
Recombinant adeno-associated virus (rAAV) gene therapy has the potential to transform the lives of patients with certain genetic disorders by increasing or restoring function to affected tissues. Following the initial establishment of transgene expression, it is unknown how long the therapeutic effect will last, although animal and emerging human data show that expression can be maintained for more than 10 years. The durability of therapeutic response is key to long-term treatment success, especially since immune responses to rAAV vectors may prevent re-dosing with the same therapy. This review explores the non-immunological and immunological processes that may limit or improve durability and the strategies that can be used to increase the duration of the therapeutic effect.
重组腺相关病毒(rAAV)基因治疗通过增加或恢复受影响组织的功能,有可能改变某些遗传疾病患者的生活。在最初建立转基因表达后,尚不清楚治疗效果会持续多长时间,尽管动物和新兴的人类数据表明表达可以维持 10 年以上。治疗反应的持久性是长期治疗成功的关键,特别是因为针对 rAAV 载体的免疫反应可能会阻止用相同的疗法再次给药。本综述探讨了可能限制或改善持久性的非免疫和免疫过程,以及可以用来增加治疗效果持续时间的策略。