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首页> 外文期刊>Journal of Autoimmunity >Anti-IL-21 monoclonal antibody combined with liraglutide effectively reverses established hyperglycemia in mouse models of type 1 diabetes
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Anti-IL-21 monoclonal antibody combined with liraglutide effectively reverses established hyperglycemia in mouse models of type 1 diabetes

机译:抗IL-21单克隆抗体与Liraglutide结合有效逆转1型糖尿病小鼠模型的高血糖症

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摘要

Abstract Immunotherapy for type 1 diabetes (T1D) has previously focused on suppressing the autoimmune response against pancreatic beta cells to preserve endogenous insulin production and regulate glucose levels. With increased attention toward combination therapy strategies, studies indicate the multifunctional cytokine interleukin-21 (IL-21) may be a suitable target as an immuno-modulatory arm, while glucagon-like peptide-1 receptor (GLP-1R) agonists may be appropriate as a beta cell protective arm in combination therapy for T1D. We report here that treatment with anti-IL-21 monoclonal antibody delays diabetes onset in the spontaneous non-obese diabetic (NOD) and NOD.scid adoptive transfer models, while its effect in reversing recent-onset hyperglycemia is limited. However, the combination of anti-IL-21 plus the GLP-1R agonist liraglutide is effective in reversing established disease compared to either monotherapy in both the NOD and rat insulin promotor-lymphocytic choriomeningitis virus glycoprotein (RIP-LCMV-GP) models of autoimmune diabetes. Enhanced efficacy is particularly evident in severely hyperglycemic mice, with return to normoglycemia remaining stable for the majority of mice even after therapy is withdrawn. Importantly, increased beta cell proliferation does not appear to be the predominant mechanism. In conclusion, combination therapy with anti-IL-21 and liraglutide is able to consistently reverse disease in mouse models of T1D. The observed effects rival the most effective experimental disease-modifying treatments tested in preclinical studies. Highlights ? Anti-IL-21 monotherapy delays diabetes in mouse models of T1D. ? Anti-IL-21?+?liraglutide reverses diabetes more effectively than either monotherapy. ? Enhanced efficacy is particularly evident in severely hyperglycemic NOD mice. ? The majority of mice remain normoglycemic following treatment withdrawal. ? Anti-IL-21?+?liraglutide is being assessed in adult recent-onset T1D (NCT02443155).
机译:摘要为1型糖尿病(T1D)的免疫疗法先前集中于抑制对胰腺β细胞的自身免疫应答,以保护内源性胰岛素产生和调节葡萄糖水平。随着联合治疗策略的提高,研究表明多官能细胞因子白细胞介素-21(IL-21)可以是作为免疫调节臂的合适靶,而胰高血糖素样肽-1受体(GLP-1R)激动剂可能是合适的作为T1D联合治疗的β细胞保护臂。在此报告,用抗IL-21单克隆抗体治疗延迟自发性非肥胖糖尿病(NOD)和NOD的糖尿病发作,而SCID养型转移模型,而其在逆转最近发病高血糖的影响是有限的。然而,抗IL-21加上GLP-1R激动剂Liraglutide的组合在NOD和大鼠胰岛素启动 - 淋巴细胞凝聚序列病毒糖蛋白(RIP-LCMV-GP)的自身免疫模型中,有效地逆转建立的疾病。糖尿病。在严重的高血糖小鼠中,增强的疗效尤其明显,甚至在疗法撤回后,恢复到大多数小鼠中剩余稳定的常见血症。重要的是,增加的β细胞增殖似乎不是主要的机制。总之,用抗IL-21和Liraglutide的组合治疗能够在T1D的小鼠模型中持续逆转疾病。观察到的效果竞争对临床研究中测试的最有效的实验性疾病改性治疗方法。强调 ?抗IL-21单药治疗延迟T1D小鼠模型中的糖尿病。还抗IL-21?+ +左旋蛋白酶比单一疗法更有效地逆转糖尿病。还在严重的高血糖NOD小鼠中,增强的疗效尤其明显。还大多数小鼠仍然是治疗戒断后的正常血糖。还抗IL-21?+?Liraglutide在成人近期发作T1D中进行评估(NCT02443155)。

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