Combined Fc-protein- and Fc-glyco-engineering of scFv-Fc fusion proteins synergistically enhances CD16a binding but does not further enhance NK-cell mediated ADCC

J Immunol Methods. 2011 Oct 28;373(1-2):67-78. doi: 10.1016/j.jim.2011.08.003. Epub 2011 Aug 9.

Abstract

Protein- or glyco-engineering of antibody molecules can be used to enhance Fc-mediated effector functions. ScFv-Fc fusion proteins (scFv-Fc) represent interesting antibody derivatives due to their relatively simple design and increased tissue penetration. Here, the impact of protein- and glyco-engineering on ADCC potency of a panel of human IgG1-based scFv-Fc was tested. Three matched sets of scFv-Fc variants targeting CD7, CD20 or HLA class II and optimized for CD16a binding by mutagenesis, lack of core-fucose, or their combination, were generated and functionally tested in comparison to the corresponding wild type scFv-Fc. Antigen binding activity was not compromised by altered glycosylation or Fc mutagenesis, whereas Fc binding to CD16a was significantly enhanced in the order: non-core fucosylated/Fc-mutated double-engineered≫Fc-mutated≥non-core-fucosylated>wild-type IgG1-Fc. All engineered variants triggered potent ADCC with up to 100-fold reduced EC50 values compared to non-engineered variants. Interestingly, double-engineered variants were similarly effective in triggering ADCC compared to single-engineered variants irrespective of their 1 log greater CD16a binding affinity. Thus, these data demonstrate that protein- and glyco-engineering enhances NK-cell mediated ADCC of scFv-Fc similarly and show that enhancing CD16a affinity beyond a certain threshold does not result in a further increase of NK-cell mediated ADCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibody Affinity / immunology
  • Antibody-Dependent Cell Cytotoxicity / immunology*
  • Antigens, CD20 / immunology
  • Antigens, CD20 / metabolism
  • Antigens, CD7 / immunology
  • Antigens, CD7 / metabolism
  • Blotting, Western
  • CHO Cells
  • Cell Line
  • Cell Line, Tumor
  • Cricetinae
  • Cricetulus
  • Flow Cytometry
  • Fucose / metabolism
  • Glycoproteins / genetics
  • Glycoproteins / immunology
  • Glycoproteins / metabolism
  • HLA-D Antigens / immunology
  • HLA-D Antigens / metabolism
  • Humans
  • Immunoglobulin Fc Fragments / genetics
  • Immunoglobulin Fc Fragments / immunology*
  • Immunoglobulin Fc Fragments / metabolism
  • Immunoglobulin G / immunology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Mutagenesis
  • Protein Binding
  • Protein Engineering / methods
  • Receptors, Fc / immunology
  • Receptors, Fc / metabolism
  • Receptors, IgG / genetics
  • Receptors, IgG / immunology*
  • Receptors, IgG / metabolism
  • Single-Chain Antibodies / genetics
  • Single-Chain Antibodies / immunology*
  • Single-Chain Antibodies / metabolism

Substances

  • Antigens, CD20
  • Antigens, CD7
  • FCGR3A protein, human
  • Glycoproteins
  • HLA-D Antigens
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Receptors, Fc
  • Receptors, IgG
  • Single-Chain Antibodies
  • Fucose