Pediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), IRCSS San Raffaele Scientific Institute, Milan, Italy; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
Pediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), IRCSS San Raffaele Scientific Institute, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy.
Hematol Oncol Clin North Am. 2022 Aug;36(4):865-878. doi: 10.1016/j.hoc.2022.03.012. Epub 2022 Jun 27.
Enzyme replacement therapy (ERT) and allogeneic hematopoietic stem cell transplantation (HSCT) are standard treatments for some mucopolysaccharidoses. Nevertheless, ERT is not curative, and HSCT is associated with significant mortality and morbidity, leaving a substantial disease burden of brain and skeletal manifestations. To overcome these limitations, different gene therapy (GT) strategies are under preclinical and clinical development. Data from ex-vivo GT clinical trials have demonstrated encouraging biochemical and early clinical outcomes. In-vivo GT, based on local brain delivery or systemic intravenous injections, resulted in biochemical and clinical stabilization of the disease.
酶替代疗法 (ERT) 和异基因造血干细胞移植 (HSCT) 是某些黏多糖贮积症的标准治疗方法。然而,ERT 并不能治愈疾病,而 HSCT 则与显著的死亡率和发病率相关,导致大脑和骨骼表现的疾病负担仍然很大。为了克服这些局限性,正在进行不同的基因治疗 (GT) 策略的临床前和临床开发。来自离体 GT 临床试验的数据显示出令人鼓舞的生化和早期临床结果。基于局部脑内递药或全身静脉注射的体内 GT 导致了疾病的生化和临床稳定。