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一种使用双功能地塞米松缀合的聚乙烯亚胺和维生素 D 结合蛋白 siRNA 的哮喘新联合疗法。

A new combination therapy for asthma using dual-function dexamethasone-conjugated polyethylenimine and vitamin D binding protein siRNA.

机构信息

Department of Bioengineering, College of Engineering, Hanyang University, Seoul, Korea.

Institute of Nano Science and Technology, Hanyang University, Seoul, Korea.

出版信息

Gene Ther. 2017 Nov;24(11):727-734. doi: 10.1038/gt.2017.83. Epub 2017 Aug 28.

Abstract

Asthma is a multifactorial disease that is influenced by the interaction of genetic and environmental factors. Because of its complex nature, there is no cure for asthma currently. Instead, reliever and controller medications are used to treat asthma. Unfortunately, conventional treatments do not work in some severe cases of asthma. In addition, there may be adverse, systemic effects of long-term treatment with high-dose inhaled corticosteroids (ICSs) as a controller medication. Therefore, we attempted to develop a novel combination therapy for asthma. Our regimen included dexamethasone as a controller medication and vitamin D binding protein (VDBP) small interfering RNA (siRNA) as a novel target therapeutic. The dexamethasone moiety of DEXA-PEI (dexamethasone-conjugated polyethylenimine) was used as an ICS, combined with anti-VDBP treatment via delivery of VDBP siRNA, using DEXA-PEI as a siRNA carrier molecule. Treatment with DEXA-PEI/VDBP siRNA effectively reduced the ovalbumin sensitization/challenge-induced enhancement of airway inflammation, goblet cell hyperplasia and expression of interleukin (IL)-4, IL-13 and CCL11. These findings suggest that the DEXA-PEI/VDBP siRNA can be developed as a potent asthma therapeutic by dose-reducing ICSs and using a multitarget therapeutic method.

摘要

哮喘是一种由遗传和环境因素相互作用影响的多因素疾病。由于其复杂性,目前尚无治愈哮喘的方法。相反,使用缓解药物和控制药物来治疗哮喘。不幸的是,在一些严重的哮喘病例中,常规治疗并不奏效。此外,长期使用高剂量吸入皮质类固醇(ICS)作为控制药物可能会产生不良反应和全身性影响。因此,我们试图开发一种新型哮喘联合治疗方法。我们的方案包括地塞米松作为控制药物和维生素 D 结合蛋白(VDBP)小干扰 RNA(siRNA)作为新型靶向治疗药物。DEXA-PEI(地塞米松缀合的聚乙烯亚胺)中的地塞米松部分用作 ICS,通过递送 VDBP siRNA 与抗 VDBP 治疗相结合,DEXA-PEI 用作 siRNA 载体分子。用 DEXA-PEI/VDBP siRNA 治疗可有效降低卵清蛋白致敏/激发诱导的气道炎症、杯状细胞增生和白细胞介素(IL)-4、IL-13 和 CCL11 的表达。这些发现表明,DEXA-PEI/VDBP siRNA 可以通过减少 ICS 剂量和使用多靶点治疗方法来开发为一种有效的哮喘治疗方法。

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