A recombinant bispecific single-chain fragment variable specific for HLA class II and Fc alpha RI (CD89) recruits polymorphonuclear neutrophils for efficient lysis of malignant B lymphoid cells

J Immunol. 2010 Feb 1;184(3):1210-7. doi: 10.4049/jimmunol.0902033. Epub 2009 Dec 30.

Abstract

Bispecific Abs offer new perspectives for cancer immunotherapy. In this study, we describe a recombinant bispecific single-chain fragment variable (bsscFv) directed against Fc alpha RI (CD89) on polymorphonuclear neutrophils (PMNs) or monocytes/macrophages and HLA class II on lymphoma target cells. Fc alpha RI and HLA class II-directed single-chain fragment variable (scFv) fragments were isolated from phage display libraries, established from the hybridomas A77 and F3.3, respectively. The two scFv molecules were connected with a 20 aa flexible linker sequence. After expression in SF21 insect cells and chromatographic purification, the bispecific molecule showed specific binding to both Ags at K(D) values of 148 +/- 42 nM and 113 +/- 25 nM for the anti-Fc alpha RI and anti-HLA class II scFv components in the bsscFv, respectively. In Ab-dependent cytotoxicity assays with PMNs as effectors and a series of lymphoma-derived cell lines (ARH-77, RAJI, REH, NALM-6, RS4;11), the bsscFv was significantly more cytotoxic than the parental murine IgG1 and its chimeric IgG1 derivative. When targeting primary tumor cell isolates from six patients with B cell malignancies, the killing capacity of the (Fc alphaRI x HLA class II) bsscFv compared favorably to conventional HLA class II mAb. Importantly, the cell lines NALM-6 and RS411, as well as two primary tumor cell isolates, were exclusively lysed by the bsscFv. To our knowledge, this is the first report of an Fc alpha RI-directed bsscFv effectively recruiting PMNs for redirected cytotoxicity against human B cell malignancies. Our data show that an (Fc alpha RI x HLA class II) bsscFv is an interesting candidate for further engineering of small, modular immunopharmaceuticals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bispecific / genetics
  • Antibodies, Bispecific / physiology*
  • Antibody-Dependent Cell Cytotoxicity* / genetics
  • Antigens, CD / genetics
  • Antigens, CD / physiology*
  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocyte Subsets / metabolism
  • B-Lymphocyte Subsets / pathology
  • Cell Line
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Movement / immunology*
  • Cricetinae
  • HLA-D Antigens / genetics
  • HLA-D Antigens / immunology*
  • Humans
  • Immunoglobulin Fragments / genetics
  • Immunoglobulin Fragments / physiology*
  • Immunoglobulin Variable Region / genetics
  • Immunoglobulin Variable Region / physiology*
  • Lymphoma, B-Cell / immunology
  • Lymphoma, B-Cell / pathology
  • Lymphoma, B-Cell / therapy
  • Mice
  • Neutrophils / immunology*
  • Neutrophils / metabolism
  • Neutrophils / pathology
  • Protein Binding / genetics
  • Protein Binding / immunology
  • Receptors, Fc / antagonists & inhibitors
  • Receptors, Fc / genetics
  • Receptors, Fc / physiology*
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / immunology*
  • Recombinant Fusion Proteins / metabolism
  • Tumor Cells, Cultured

Substances

  • Antibodies, Bispecific
  • Antigens, CD
  • Fc(alpha) receptor
  • HLA-D Antigens
  • Immunoglobulin Fragments
  • Immunoglobulin Variable Region
  • Receptors, Fc
  • Recombinant Fusion Proteins
  • immunoglobulin Fv