Xie Aini, Li Rongying, Jiang Tao, Yan Hui, Zhang Hedong, Yang Yisheng, Yang Lina, Yechoor Vijay, Chan Lawrence, Chen Wenhao
Center for Immunobiology and Transplantation Research, Department of Surgery, Houston Methodist Research Institute, Houston Methodist Hospital, Houston, Texas 77030.
Division of Diabetes, Endocrinology & Metabolism, Diabetes & Endocrinology Research Center, Department of Medicine, Baylor College of Medicine, Houston, Texas 77030.
Endocrinology. 2017 Oct 1;158(10):3140-3151. doi: 10.1210/en.2016-1947.
Insulin-producing β cells in patients with type 1 diabetes (T1D) are destroyed by T lymphocytes. We investigated whether targeting the T-cell receptor (TCR) with a monoclonal antibody (mAb) abrogates T-cell response against residual and newly formed islets in overtly diabetic nonobese diabetic (NOD) mice. NOD mice with blood glucose levels of 250 to 350 mg/dL or 350 to 450 mg/dL were considered as new-onset or established overt diabetes, respectively. These diabetic NOD mice were transiently treated with an anti-TCR β chain (TCRβ) mAb, H57-597, for 5 days. Two weeks later, some NOD mice with established overt diabetes further received hepatic gene therapy using the islet-lineage determining gene Neurogenin3 (Ngn3), in combination with the islet growth factor gene betacellulin (Btc). We found that anti-TCRβ mAb (50 µg/d) reversed >80% new-onset diabetes in NOD mice for >14 weeks by reducing the number of effector T cells in the pancreas. However, anti-TCRβ mAb therapy alone reversed only ∼20% established overt diabetes in these mice. Among those overtly diabetic NOD mice whose diabetes was resistant to anti-TCRβ mAb treatment, ∼60% no longer had diabetes when they also received Ngn3-Btc hepatic gene transfer 2 weeks after initial anti-TCRβ mAb treatment. This combination of Ngn3-Btc gene therapy and anti-TCRβ mAb treatment induced the sustained formation of periportal insulin-producing cells in the liver of overtly diabetic mice. Therefore, directly targeting TCRβ with a mAb potently reverses new-onset T1D in NOD mice and protects residual and newly formed gene therapy-induced hepatic neo-islets from T-cell‒mediated destruction in mice with established overt diabetes.
1型糖尿病(T1D)患者中产生胰岛素的β细胞被T淋巴细胞破坏。我们研究了用单克隆抗体(mAb)靶向T细胞受体(TCR)是否能消除显性糖尿病非肥胖糖尿病(NOD)小鼠针对残留和新形成胰岛的T细胞反应。血糖水平为250至350mg/dL或350至450mg/dL的NOD小鼠分别被视为新发或已确诊的显性糖尿病。这些糖尿病NOD小鼠用抗TCRβ链(TCRβ)mAb H57-597进行了5天的短暂治疗。两周后,一些已确诊显性糖尿病的NOD小鼠进一步接受了使用胰岛谱系决定基因Neurogenin3(Ngn3)与胰岛生长因子基因β细胞ulin(Btc)的肝脏基因治疗。我们发现,抗TCRβ mAb(50μg/d)通过减少胰腺中效应T细胞的数量,使NOD小鼠中超过80%的新发糖尿病逆转超过14周。然而,单独使用抗TCRβ mAb治疗仅使这些小鼠中约20%的已确诊显性糖尿病得到逆转。在那些对抗TCRβ mAb治疗耐药性糖尿病的显性糖尿病NOD小鼠中,约60%在初次抗TCRβ mAb治疗2周后接受Ngn3-Btc肝脏基因转移时不再患有糖尿病。Ngn3-Btc基因治疗与抗TCRβ mAb治疗的这种联合诱导了显性糖尿病小鼠肝脏中门静脉周围产生胰岛素细胞的持续形成。因此,用mAb直接靶向TCRβ可有效逆转NOD小鼠的新发T1D,并保护残留和新形成的基因治疗诱导的肝脏新胰岛免受已确诊显性糖尿病小鼠中T细胞介导的破坏。