血液造血干细胞基因治疗神经代谢性溶酶体储存疾病的基因治疗

Giulia Consiglieri1, Francesca Tucci1, Maria Ester Bernardo2

  • 1Pediatric Immunohematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, Milan, Italy; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Milan, Italy.

Brain & development
|June 26, 2025
PubMed
概括

造血干细胞原始细胞基因疗法 (HSPC-GT) 为罕见的神经代谢疾病提供了一个有前途的新疗法. 这种创新方法利用患者自己的细胞提供治疗基因,解决其他治疗方法不足的未满足需求.

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