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IMAGING-AIDED GENE THERAPY USING MESENCHYMAL STEM CELLS AS TARGET-DELIVERY VEHICLE

机译:以间充质干细胞为靶标传递载体的影像辅助基因治疗

摘要

Compositions and methods of use thereof encompass engineered mesenchymal stem cells as a vehicle to deliver secreted tissue necrosis factor-RGD4C fusion polypeptides for tumor treatment, thereby reducing side effects of TNF. A reporter gene can be included in vector constructs to monitor the localization and viability of engineered MSCs after administration into a recipient animal. The genetically modified mesenchymal stem cell can comprise an expression cassette comprising a nucleic acid sequence operably linked to a gene expression promoter and encoding the heterologous fusion polypeptide comprising a tissue necrotic factor region and an integrin-binding region. Another aspect of the disclosure encompasses embodiments of a method of modulating the proliferation of a targeted population of tumor cells by delivering a population of the genetically modified mesenchymal stem cells to tumor cells, allowing the mesenchymal stem cells to express the heterologous polypeptide, thereby reducing the proliferative capacity of the tumor cells.
机译:其组合物和使用方法包括工程化的间充质干细胞作为载体,以递送分泌的组织坏死因子-RGD4C融合多肽用于肿瘤治疗,从而减少TNF的副作用。可以在载体构建体中包括报告基因,以监测施用给受体动物后工程化的MSC的定位和生存力。遗传修饰的间充质干细胞可包含表达盒,该表达盒包含与基因表达启动子可操作地连接的核酸序列,并编码包含组织坏死因子区域和整联蛋白结合区域的异源融合多肽。本公开内容的另一方面包括通过将遗传修饰的间充质干细胞群递送至肿瘤细胞,从而使间充质干细胞表达异源多肽,从而减少肿瘤细胞,从而调节靶定肿瘤细胞群增殖的方法的实施方案。肿瘤细胞的增殖能力。

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