A novel glycoengineered bispecific antibody format for targeted inhibition of epidermal growth factor receptor (EGFR) and insulin-like growth factor receptor type I (IGF-1R) demonstrating unique molecular properties

J Biol Chem. 2014 Jul 4;289(27):18693-706. doi: 10.1074/jbc.M113.528109. Epub 2014 May 19.

Abstract

In the present study, we have developed a novel one-arm single chain Fab heterodimeric bispecific IgG (OAscFab-IgG) antibody format targeting the insulin-like growth factor receptor type I (IGF-1R) and the epidermal growth factor receptor (EGFR) with one binding site for each target antigen. The bispecific antibody XGFR is based on the "knob-into-hole" technology for heavy chain heterodimerization with one heavy chain consisting of a single chain Fab to prevent wrong pairing of light chains. XGFR was produced with high expression yields and showed simultaneous binding to IGF-1R and EGFR with high affinity. Due to monovalent binding of XGFR to IGF-1R, IGF-1R internalization was strongly reduced compared with the bivalent parental antibody, leading to enhanced Fc-mediated cellular cytotoxicity. To further increase immune effector functions triggered by XGFR, the Fc portion of the bispecific antibody was glycoengineered, which resulted in strong antibody-dependent cell-mediated cytotoxicity activity. XGFR-mediated inhibition of IGF-1R and EGFR phosphorylation as well as A549 tumor cell proliferation was highly effective and was comparable with a combined treatment with EGFR (GA201) and IGF-1R (R1507) antibodies. XGFR also demonstrated potent anti-tumor efficacy in multiple mouse xenograft tumor models with a complete growth inhibition of AsPC1 human pancreatic tumors and improved survival of SCID beige mice carrying A549 human lung tumors compared with treatment with antibodies targeting either IGF-1R or EGFR. In summary, we have applied rational antibody engineering technology to develop a heterodimeric OAscFab-IgG bispecific antibody, which combines potent signaling inhibition with antibody-dependent cell-mediated cytotoxicity induction and results in superior molecular properties over two established tetravalent bispecific formats.

Keywords: Antibody Engineering; Epidermal Growth Factor Receptor (EGFR); Glycosylation; Insulin-like Growth Factor (IGF); Tumor Therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bispecific / chemistry
  • Antibodies, Bispecific / immunology*
  • Antibodies, Bispecific / metabolism
  • Antibodies, Bispecific / pharmacology
  • Binding Sites
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • ErbB Receptors / immunology*
  • ErbB Receptors / metabolism
  • Female
  • Gene Expression Regulation / drug effects
  • Glycosylation
  • Humans
  • Immunoglobulin G / chemistry
  • Immunoglobulin G / immunology*
  • Immunoglobulin G / metabolism
  • Immunoglobulin G / pharmacology
  • Mice
  • Pancreatic Neoplasms / pathology
  • Protein Engineering*
  • Protein Multimerization
  • Protein Structure, Quaternary
  • Protein Transport / drug effects
  • Receptor, IGF Type 1 / immunology*
  • Receptor, IGF Type 1 / metabolism
  • Signal Transduction / drug effects
  • Single-Chain Antibodies / chemistry
  • Single-Chain Antibodies / immunology*
  • Single-Chain Antibodies / metabolism
  • Single-Chain Antibodies / pharmacology
  • Xenograft Model Antitumor Assays

Substances

  • Antibodies, Bispecific
  • Immunoglobulin G
  • Single-Chain Antibodies
  • ErbB Receptors
  • Receptor, IGF Type 1