Eladocagene exuparvovec gene therapy improves motor development in patients with aromatic L-amino acid decarboxylase deficiency

P. Hwu, A. Roubertie, Y. Chien, Ni‐Chung Lee, Antonia Wang, Alexis Russell, P.E. Pachelli, L. Giugliani, A. Federhen, Chun-Hwei Tai
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Abstract

Introduction: Aromatic L-amino acid decarboxylase (AADC) deficiency is caused by mutations in the DDC gene reducing AADC enzyme activity causing motor and neurodevelopmental impairments. Objectives: Evaluate clinical outcomes in children with AADC treated with Eladocagene exuparvovec, recombinant adeno-associated viral vector serotype 2 carrying the coding sequence for AADC enzyme. Methods: Therapy was infused bilaterally in the putamina of 30 patients aged 18–102 months receiving 1.8 × 1011 vg (n = 21) or 2.4 × 1011 vg (n = 9) followed for up to 120 months assessed using PDMS-2 key motor milestones including head control (partial or full), sitting (supported or independently), standing (with/away from support; up from cross-legged position), and walking (with/ without assistance; 10 feet; taped line). Motor milestones were measured every 3 months for 1 year following gene therapy, then every 6–12 months for ≤ 120 months. Data extracted on January 4, 2022. Results: At baseline, no patients had mastered head control or more advanced milestones. At year 1 of follow-up, patients were gaining the following skills (n): partial head control (26); full head control (15), sitting unassisted (7), supported standing (2). Progression of development was noted at years 5 and 10. By year 5 of follow-up, more advanced milestones were achieved (n): full head control (24), sitting unassisted (21) assisted walking (5), walking 10 feet (3), or walking upstairs (3). These abilities were maintained for as long as 10 years. Conclusion: The data indicate that eladocagene exuparvovec can provide a durable, positive impact on motor development in patients with AADC deficiency
艾拉多卡金exuparvovec基因疗法可改善芳香族L-氨基酸脱羧酶缺乏症患者的运动发育状况
简介芳香族 L-氨基酸脱羧酶(AADC)缺乏症是由于 DDC 基因突变导致 AADC 酶活性降低,从而引起运动和神经发育障碍。研究目标评估使用携带 AADC 酶编码序列的重组腺相关病毒载体血清 2 型 Eladocagene exuparvovec 治疗 AADC 儿童的临床疗效。治疗方法对30名年龄在18-102个月的患者进行双侧输注治疗,患者接受1.8 × 1011 vg(n = 21)或2.4 × 1011 vg(n = 9)的治疗,随访时间长达120个月,使用PDMS-2关键运动里程碑进行评估,包括头部控制(部分或全部)、坐(有支撑或独立)、站立(有支撑/离开支撑;从盘腿姿势站起)和行走(有辅助/无辅助;10英尺;绑线)。在基因治疗后的 1 年内,每 3 个月测量一次运动发育里程碑,之后每 6-12 个月测量一次,直至 120 个月。数据提取日期为 2022 年 1 月 4 日。结果:基线时,没有患者掌握头部控制或更高级的里程碑。在随访的第一年,患者掌握了以下技能(n):部分头部控制(26);完全头部控制(15),无助坐立(7),支撑站立(2)。在第 5 年和第 10 年,患者的能力得到了进一步提高。到随访的第 5 年,他们达到了更高的里程碑(n):完全头部控制(24)、无辅助坐立(21)、辅助行走(5)、行走 10 英尺(3)或上楼行走(3)。这些能力保持了 10 年之久。结论这些数据表明,艾拉多卡金exuparvovec能对AADC缺乏症患者的运动发育产生持久、积极的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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