細胞表面接着型インターフェロンを利用した標的特異的作用型遺伝子治療システムの開発
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Interferon-γ (IFN-γ) is a type II IFN that possesses various biological activities including antivirus effect and antitumor effect. Because of its potent biological activities, IFN-γ has been used as a therapeutic treatment for cancer patients and is expected to be a therapeutic for other diseases. As the half-life of IFN-γ in blood circulation is very short, IFN-γ gene therapy, in which IFN-γ gene is used to continuously supply IFN-γ protein, is a promising approach because it can continuously supply IFN-γ. To improve therapeutic effect of IFN-γ-based gene therapy, it is important to control the spatiotemporal distribution of IFN-γ expressed from the plasmid DNA vector encoding IFN-γ. We developed a method to regulate the time profile of IFN-γ expressed from plasmid DNA by modifying vector backbone. In addition, we developed a method that can increase retention time of IFN-γ in blood circulation by designing IFN-γ encoded in plasmid vector as a fusion protein with mouse serum albumin (MSA). Regulation of time profile of IFN-γ expression was highly effective in avoiding unwanted effect of IFN-γ without decreasing therapeutic effect. In addition, gene delivery of MSA-IFN-γ fusion protein increased retention time of IFN-γ in blood circulation than native IFN-γ gene delivery did. Thus, designing both plasmid vector and therapeutic protein encoded by the vector is a promising approach to controlling the spatiotemporal distribution of proteins which can increase the therapeutic potency of IFN-γ-based gene therapy as well as safety of in vivo IFN-γ gene therapy.
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