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Methods and Reagents for effective and targeted gene transfer to monocytes and macrophages

机译:有效和靶向基因转移至单核细胞和巨噬细胞的方法和试剂

摘要

Useful and biosecure vector to transfer genetic material to CD14 + mononuclear Cells (monocytes and monocyte derived macrophages) in an effective way and specific. The Implementation makes use of the Chimeric Human adenovirus 5 vector carrying Short Fibre ad40 enterotropico to transfer genetic material to target CD14 + mononuclear cells.Claim 3: in vitro procedure to provide a compound of interest in a monocyte macrophage Cell Lineage comprising contacting Said cell with a nanocarrier that carries the compound of interest and the carrier contains at least one part d Short Fibre and Protein of adenovirus Group f or a functionally equivalent variantSame. Claim 1: nanocarrier that includes a product of interest and at least a part of the Short Fiber Protein of adenovirus Subgroup f or a functionally equivalent Variant thereof for use in the treatment of a disease Associated Cell Lineage monoci Cough - macrophages.
机译:有用且生物安全的载体,可以有效且特异性地将遗传物质转移至CD14 +单核细胞(单核细胞和单核细胞衍生的巨噬细胞)。该实施方案利用携带短纤维ad40嗜肠性粒细胞的嵌合人类腺病毒5载体将遗传物质转移到目标CD14 +单核细胞中。权利要求3:体外程序在单核巨噬细胞细胞谱系中提供目标化合物,包括使所述细胞与载有目标化合物的纳米载体,并且该载体至少包含d腺病毒组f的短纤维和蛋白质或功能相同的变异体相同的至少一部分。权利要求1:纳米载体,其包括感兴趣的产物和腺病毒f亚群f的短纤维蛋白的至少一部分或其功能上等效的变体,用于治疗疾病相关的细胞谱系单胞菌咳嗽-巨噬细胞。

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