Department of Green Bioengineering, Korea National University of Transportation, Chungju 27469, Republic of Korea.
KB BioMed Inc., Chungju 27469, Republic of Korea.
ACS Appl Mater Interfaces. 2020 Sep 2;12(35):38925-38935. doi: 10.1021/acsami.0c09814. Epub 2020 Aug 19.
Type 2 diabetes mellitus (T2DM) is a chronic and progressive hyperglycemic condition. Glucagon-like peptide-1 (GLP1) is an incretin secreted from pancreatic β-cells and helps to produce insulin to balance the blood glucose level without the risk of hypoglycemia. However, the therapeutic application of GLP1 is limited by its intrinsic short half-life and rapid metabolic clearance in the body. To enhance the antidiabetic effect of GLP1, we designed a human cysteine-modified IgG1-Fc antibody-mediated oral gene delivery vehicle, which helps to produce GLP1 sustainably in the target site with the help of increased half-life of the Fc-conjugated nanocarrier, protects GLP1 from acidic and enzymatic degradation in the gastrointestinal (GI) tract, uptakes and transports the GLP1 formulation through the neonatal Fc receptor (FcRn), and helps to release the GLP1 gene in the intestine. Our formulation could reduce the blood glucose from about an average of 320 mg/dL (hyperglycemic) to 150 mg/dL (normal blood glucose concentration) in diabetic mice, which is about 50% reduction of the total blood glucose concentration. GLP1 (500 μg) complexed with the IgG1-Fc carrier was proven to be the optimal dose for a complete reduction of hyperglycemic conditions in diabetic mice. A significant amount of insulin production and the presence of GLP1 peptide were observed in the pancreatic islets of oral GLP1 formulation-treated diabetic mice in immunohistochemistry analysis compared to nontreated diabetic mice. The orally given formulation was completely nontoxic according to the histopathology analysis of mice organ tissues, and no mice death was observed. Our antibody-mediated oral gene delivery system is a promising tool for various oral therapeutic gene delivery applications to treat diseases like diabetes.
2 型糖尿病(T2DM)是一种慢性进行性高血糖状态。胰高血糖素样肽-1(GLP1)是一种由胰岛β细胞分泌的肠促胰岛素,有助于产生胰岛素来平衡血糖水平,而不会有低血糖的风险。然而,GLP1 的治疗应用受到其内在的短半衰期和在体内快速代谢清除的限制。为了增强 GLP1 的抗糖尿病作用,我们设计了一种人半胱氨酸修饰的 IgG1-Fc 抗体介导的口服基因传递载体,该载体有助于在目标部位持续产生 GLP1,借助增加 Fc 缀合纳米载体的半衰期来保护 GLP1 免受胃肠道(GI)道中的酸性和酶降解,通过新生儿 Fc 受体(FcRn)摄取和转运 GLP1 制剂,并有助于在肠道中释放 GLP1 基因。我们的制剂可以将糖尿病小鼠的血糖从平均约 320mg/dL(高血糖)降低到 150mg/dL(正常血糖浓度),约为总血糖浓度的 50%降低。在糖尿病小鼠中,证明与 IgG1-Fc 载体复合的 GLP1(500μg)是完全降低高血糖状态的最佳剂量。与未治疗的糖尿病小鼠相比,在口服 GLP1 制剂治疗的糖尿病小鼠的免疫组织化学分析中,胰岛中观察到大量胰岛素的产生和 GLP1 肽的存在。根据小鼠器官组织的组织病理学分析,口服给予的制剂完全无毒,没有观察到小鼠死亡。我们的抗体介导的口服基因传递系统是一种有前途的工具,可用于各种口服治疗性基因传递应用,以治疗糖尿病等疾病。