A Fully Human, Allosteric Monoclonal Antibody That Activates the Insulin Receptor and Improves Glycemic Control

作者：Bhaskar Vinay^*; Goldfine Ira D; Bedinger Daniel H; Lau Angela; Kuan Hua F; Gross Lisa M; Handa Masahisa; Maddux Betty A; Watson Susan R; Zhu Shirley; Narasimha Ajay J; Levy Raphael; Webster Lynn; Wijesuriya Sujeewa D; Liu Naichi; Wu Xiaorong; Chemla Vogel David; Catarina Tran; Lee Steve R; Wong Steve; Wilcock Diane; White Mark L; Corbin John A

来源：Diabetes, 2012, 61(5): 1263-1271.

DOI：10.2337/db11-1578

Many patients with diabetes mellitus (both type 1 and type 2) require therapy to maintain normal fasting glucose levels. To develop a novel treatment for these individuals, we used phage display technology to target the insulin receptor (INSR) complexed with insulin and identified a high affinity, allosteric, human monoclonal antibody, XMetA, which mimicked the glucoregulatory, but not the mitogenic, actions of insulin. Biophysical studies with cultured cells expressing human INSR demonstrated that XMetA acted allosterically and did not compete with insulin for binding to its receptor. XMetA was found to function as a specific partial agonist of INSR, eliciting tyrosine phosphorylation of INSR but not the IGF-IR. Although this antibody activated metabolic signaling, leading to enhanced glucose uptake, it neither activated Erk nor induced proliferation of cancer cells. In an insulin resistant, insulinopenic model of diabetes, XMetA markedly reduced elevated fasting blood glucose and normalized glucose tolerance. After 6 weeks, significant improvements in HbA(1c), dyslipidemia, and other manifestations of diabetes were observed. It is noteworthy that hypoglycemia and weight gain were not observed during these studies. These studies indicate, therefore, that allosteric monoclonal antibodies have the potential to be novel, ultra-long acting, agents for the regulation of hyperglycemia in diabetes. Diabetes 61:1263-1271, 2012

• 出版日期2012-5