Cell Transplantation (Jun 2015)

Depletion of Alloreactive T-Cells by Anti-CD137-Saporin Immunotoxin

  • Sang C. Lee,
  • Kwang W. Seo,
  • Hye J. Kim,
  • Sang W. Kang,
  • Hye-Jeong Choi,
  • Ansuk Kim,
  • Byoung S. Kwon,
  • Hong R. Cho,
  • Byungsuk Kwon

DOI
https://doi.org/10.3727/096368914X679327
Journal volume & issue
Vol. 24

Abstract

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Depletion of alloreactive T-lymphocytes from allogeneic bone marrow tansplants may prevent graft-versus-host disease (GVHD) without impairing donor cell engraftment, immunity, and the graft-versus-leukemia (GVL) effect. Alloreactive T-cells may be identified by their expression, upon activation, of CD137, a costimulatory receptor and putative surrogate marker for antigen-specific effector T-cells. In this context, we tested the use of anti-CD137-saporin immunotoxin to selectively deplete mouse and human alloreactive T-cells. Anti-CD137 antibodies were internalized by cells within 4 h of binding to the cell surface CD137, and anti-CD137-saporin immunotoxin effectively killed polyclonally activated T-cells or antigen-stimulated T-cells. Transfer of donor T-cells after allodepletion with anti-CD137-saporin immunotoxin failed to induce any evident expression of GVHD; however, a significant GVL effect was observed. Targeting of CD137 with an immunotoxin was also effective in killing polyclonally activated or alloreactive human T-cells. Our results indicate that anti-CD137-saporin immunotoxin may be used to deplete alloreactive T-cells prior to bone marrow transplantation and thereby prevent GVHD and the relapse of leukemia.