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2-二乙氨基乙基-葡聚糖甲基丙烯酸甲酯共聚物非病毒载体:气溶胶基因治疗的安全性仍有很长的路要走。

2-diethylaminoethyl-dextran methyl methacrylate copolymer nonviral vector: still a long way toward the safety of aerosol gene therapy.

机构信息

1] Pulmonary Department-Oncology Unit, 'G. Papanikolaou' General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece [2] Department of Interventional Pneumology, Ruhrlandklinik, West German Lung Center, University Hospital, University Duisburg-Essen, Essen, Germany.

出版信息

Gene Ther. 2013 Oct;20(10):1022-8. doi: 10.1038/gt.2013.27. Epub 2013 May 30.

DOI:10.1038/gt.2013.27
PMID:23719068
Abstract

Revealing the lung tumor genome has directed the current treatment strategies toward targeted therapy. First line treatments targeting the genome of lung tumor cells have been approved and are on the market. However, they are limited by the small number of patients with the current investigated genetic mutations. Novel treatment administration modalities have been also investigated in an effort to increase the local drug deposition and disease control. In the current study, we investigated the safety of the new nonviral vector 2-diethylaminoethyl-dextran methyl methacrylate copolymer (DDMC; Ryujyu Science), which belongs to the 2-diethylaminoethyl-dextran family by aerosol administration. Thirty male BALBC mice, 2 month old, were included and divided into three groups. However, pathological findings indicated severe emphysema within three aerosol sessions. In addition, the CytoViva technique was applied for the first time to display the nonviral particles within the pulmonary tissue and emphysema lesions, and a spectral library of the nonviral vector was also established. Although our results in BALBC mice prevented us from further investigation of the DDMC nonviral vector as a vehicle for gene therapy, further investigation in animals with larger airways is warranted to properly evaluate the safety of the vector.

摘要

揭示肺部肿瘤基因组指导了当前针对靶向治疗的治疗策略。针对肺部肿瘤细胞基因组的一线治疗方法已被批准并上市。然而,它们受到目前研究的遗传突变患者数量较少的限制。为了增加局部药物沉积和疾病控制,还研究了新的治疗给药方式。在目前的研究中,我们研究了新型非病毒载体 2-二乙氨基乙基-葡聚糖甲基丙烯酸甲酯共聚物(DDMC;Ryujyu Science)通过气溶胶给药的安全性。我们纳入了 30 只 2 个月大的雄性 BALBC 小鼠,并将其分为三组。然而,病理发现表明在三次气溶胶治疗后出现严重的肺气肿。此外,我们首次应用 CytoViva 技术显示肺部组织和肺气肿病变中的非病毒颗粒,并建立了非病毒载体的光谱库。尽管我们在 BALBC 小鼠中的结果阻止了我们进一步将 DDMC 非病毒载体作为基因治疗的载体进行研究,但需要在具有更大气道的动物中进一步研究,以正确评估载体的安全性。

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