调节AAV9银糖结合率产生了新型基因疗法载体,并预测了甘氨酸贪的跨物种差异

Jacob A Hoffman1, Nathan Denton1, Joshua J Sims1

  • 1Gene Therapy Program, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Human gene therapy
|July 13, 2024
PubMed
概括

研究人员设计了腺相关病毒 (AAV) 变体,以减少肝脏积累并增强心脏基因递送. 这种新型HRH变异显示出更安全,更有效的针对肝外组织的AAV基因疗法的前景.