Chang Alex H, Stephan Matthias T, Sadelain Michel
Laboratory of Gene Transfer and Gene Expression, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Nat Biotechnol. 2006 Aug;24(8):1017-21. doi: 10.1038/nbt1227. Epub 2006 Jul 16.
We demonstrate here the capacity of erythroid cells to mediate long-term, systemic and therapeutic protein delivery in vivo. By targeting human factor IX (hFIX) expression to late-stage erythropoiesis, we achieve long-term hFIX secretion at levels significantly higher (>tenfold) than those obtained with an archetypal ubiquitous promoter in a mouse model of hemophilia B. Erythroid cell-derived hFIX is biologically active, resulting in phenotypic correction of the bleeding disorder. In addition to achieving high expression levels and resistance to transcriptional silencing, red cell-mediated protein delivery offers multiple advantages including immune tolerance induction, reduction of the risk of insertional oncogenesis and relative ease of application by either engrafting transduced hematopoietic stem cells or transfusing ex vivo-generated, stem cell-derived erythroid cells.
我们在此证明了红细胞在体内介导长期、全身性和治疗性蛋白质递送的能力。通过将人凝血因子IX(hFIX)的表达靶向晚期红细胞生成,我们在B型血友病小鼠模型中实现了长期hFIX分泌,其水平显著高于(>10倍)使用典型的遍在启动子所获得的水平。红细胞衍生的hFIX具有生物活性,可导致出血性疾病的表型纠正。除了实现高表达水平和抗转录沉默外,红细胞介导的蛋白质递送还具有多种优势,包括诱导免疫耐受、降低插入性肿瘤发生的风险以及通过移植转导的造血干细胞或输注体外生成的、干细胞衍生的红细胞相对容易应用。