Dénes Béla, Yu Jie, Fodor Nadja, Takátsy Zsuzsanna, Fodor István, Langridge William H R
Center for Molecular Biology and Gene Therapy, Department of Biochemistry and Microbiology, Loma Linda University, Loma Linda, CA 92350, USA.
Mol Biotechnol. 2006 Nov;34(3):317-27. doi: 10.1385/MB:34:3:317.
In autoimmune (type 1) diabetes, autoreactive lymphocytes destroy pancreatic beta-cells responsible for insulin synthesis. To assess the feasibility of gene therapy for type 1 diabetes, recombinant vaccinia virus (rVV) vectors were constructed expressing pancreatic islet autoantigens proinsulin (INS) and a 55-kDa immunogenic peptide from glutamic acid decarboxylase (GAD), and the immunomodulatory cytokine interleukin (IL)-10. To augment the beneficial effects of recombinant virus therapy, the INS and GAD genes were fused to the C terminus of the cholera toxin B subunit (CTB). Five-week-old non-obese diabetic (NOD) mice were injected once with rVV. Humoral antibody immune responses and hyperglycemia in the infected mice were analyzed. Only 20% of the mice inoculated with rVV expressing the CTB::INS fusion protein developed hyperglycemia, in comparison to 70% of the mice in the uninoculated animal group. Islets from pancreatic tissues isolated from euglycemic mice from this animal group showed no sign of inflammatory lymphocyte invasion. Inoculation with rVV producing CTB::GAD or IL-10 was somewhat less effective in reducing diabetes. Humoral antibody isotypes of hyperglycemic and euglycemic mice from all treated groups possessed similar IgG1/IgG2c antibody titer ratios from 19 to 32 wk after virus inoculation. In comparison with uninoculated mice, 11-wk-old NOD mice injected with virus expressing CTB::INS were delayed in diabetes onset by more than 4 wk. The experimental results demonstrate the feasibility of using rVV expressing CTB::INS fusion protein to generate significant protection and therapy against type 1 diabetes onset and progression.
在自身免疫性(1型)糖尿病中,自身反应性淋巴细胞会破坏负责胰岛素合成的胰腺β细胞。为了评估1型糖尿病基因治疗的可行性,构建了重组痘苗病毒(rVV)载体,其表达胰岛自身抗原胰岛素原(INS)和来自谷氨酸脱羧酶(GAD)的55 kDa免疫原性肽,以及免疫调节细胞因子白细胞介素(IL)-10。为了增强重组病毒治疗的有益效果,将INS和GAD基因融合到霍乱毒素B亚基(CTB)的C末端。给5周龄的非肥胖糖尿病(NOD)小鼠单次注射rVV。分析感染小鼠的体液抗体免疫反应和高血糖情况。与未接种动物组中70%的小鼠相比,接种表达CTB::INS融合蛋白的rVV的小鼠中只有20%出现高血糖。从该动物组血糖正常的小鼠分离的胰腺组织中的胰岛没有炎症淋巴细胞浸润的迹象。接种产生CTB::GAD或IL-10的rVV在降低糖尿病发生率方面效果稍差。在病毒接种后19至32周,所有治疗组中血糖高和血糖正常的小鼠的体液抗体亚型具有相似的IgG1/IgG2c抗体滴度比。与未接种小鼠相比,注射表达CTB::INS病毒的11周龄NOD小鼠的糖尿病发病延迟了4周以上。实验结果证明了使用表达CTB::INS融合蛋白的rVV对1型糖尿病的发病和进展产生显著保护和治疗作用的可行性。