Selective elimination of human regulatory T lymphocytes in vitro with the recombinant immunotoxin LMB-2

J Immunother. 2006 Mar-Apr;29(2):208-14. doi: 10.1097/01.cji.0000187959.45803.0c.

Abstract

CD4(+)CD25(+) T-regulatory cells (T(reg)) can inhibit the proliferation and cytokine secretion of CD4(+)CD25(-) helper T cells in mice and humans. In murine tumor models, the presence of these T(reg) cells can inhibit the antitumor effectiveness of T-cell transfer and active immunization approaches. We have thus initiated efforts to eliminate T(reg) cells selectively from human peripheral blood mononuclear cells (PBMCs) to potentially bolster antitumor responses. LMB-2 is a recombinant immunotoxin that is a fusion of a single-chain Fv fragment of the anti-Tac anti-CD25 monoclonal antibody to a truncated form of the bacterial Pseudomonas exotoxin A. In vitro incubation of human PBMCs with LMB-2 reduced the levels of CD4(+)CD25(+) and Foxp3-expressing cells without impairing the function of the remaining lymphocytes. The short in vivo half-life of LMB-2 makes it an attractive candidate for reducing human T(reg) cells in vivo before the administration of cancer vaccine or cell transfer immunotherapy approaches.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal / immunology
  • CD4 Antigens / immunology
  • Cancer Vaccines
  • Cell Death / immunology
  • Cells, Cultured
  • Exotoxins / administration & dosage
  • Exotoxins / immunology
  • Humans
  • Immunotherapy
  • Immunotoxins / administration & dosage*
  • Immunotoxins / immunology
  • Lymphocyte Depletion / methods
  • Mice
  • Receptors, Interleukin-2 / immunology
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / immunology
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / pathology

Substances

  • Antibodies, Monoclonal
  • B3(Fv)-PE38KDEL recombinant immunotoxin
  • CD4 Antigens
  • Cancer Vaccines
  • Exotoxins
  • Immunotoxins
  • Receptors, Interleukin-2
  • Recombinant Proteins