Killer artificial antigen-presenting cells: a novel strategy to delete specific T cells

Blood. 2008 Apr 1;111(7):3546-52. doi: 10.1182/blood-2007-09-113522. Epub 2007 Dec 20.

Abstract

Several cell-based immunotherapy strategies have been developed to specifically modulate T cell-mediated immune responses. These methods frequently rely on the utilization of tolerogenic cell-based antigen-presenting cells (APCs). However, APCs are highly sensitive to cytotoxic T-cell responses, thus limiting their therapeutic capacity. Here, we describe a novel bead-based approach to modulate T-cell responses in an antigen-specific fashion. We have generated killer artificial APCs (kappaaAPCs) by coupling an apoptosis-inducing alpha-Fas (CD95) IgM mAb together with HLA-A2 Ig molecules onto beads. These kappaaAPCs deplete targeted antigen-specific T cells in a Fas/Fas ligand (FasL)-dependent fashion. T-cell depletion in cocultures is rapidly initiated (30 minutes), dependent on the amount of kappaaAPCs and independent of activation-induced cell death (AICD). kappaaAPCs represent a novel technology that can control T cell-mediated immune responses, and therefore has potential for use in treatment of autoimmune diseases and allograft rejection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / immunology*
  • Antigen-Presenting Cells / chemistry
  • Antigen-Presenting Cells / immunology*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / therapy
  • Cell Death / immunology
  • Cells, Cultured
  • Fas Ligand Protein / immunology
  • Graft Rejection / immunology
  • Graft Rejection / therapy
  • Humans
  • Immune Tolerance*
  • Immunoglobulin M / chemistry
  • Immunoglobulin M / immunology*
  • Lymphocyte Depletion / methods*
  • Microspheres*
  • T-Lymphocytes, Cytotoxic / immunology*
  • Time Factors
  • Transplantation, Homologous
  • fas Receptor / chemistry
  • fas Receptor / immunology*

Substances

  • Antibodies, Monoclonal
  • Fas Ligand Protein
  • Immunoglobulin M
  • fas Receptor