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Immune responses, not promoter inactivation, are responsible for decreased long‐term expression following plasmid gene transfer into skeletal muscle

机译:免疫反应,而不是启动子失活,是质粒基因转移到骨骼肌后长期表达降低的原因

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Long-term high-level in vivo gene expression appears to depend on the promoter chosen to drive the gene of choice. In many cases the promoter appears to ‘switch off’ some time after in vivo gene transfer. We demonstrate that, following intramuscular injection of β-galactosidase reporter plasmids, promoter ‘switch off’ is due to elimination of fibres expressing the transferred reporter gene by activation of a Th1 (cytotoxic) immune response. This finding, in the absence of stimulation of the immune system by viral vector proteins, has implications not only for gene transfer experiments but for the future of muscle-directed gene therapy.
机译:长期高水平的体内基因表达似乎取决于选择驱动所选基因的启动子。在许多情况下,启动子似乎在体内基因转移后的一段时间内“关闭”。我们证明,在肌内注射 β-半乳糖苷酶报告质粒后,启动子“关闭”是由于通过激活 Th1(细胞毒性)免疫反应消除了表达转移的报告基因的纤维。在病毒载体蛋白没有刺激免疫系统的情况下,这一发现不仅对基因转移实验有影响,而且对肌肉定向基因治疗的未来也有影响。

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