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Cell Transplant ; 24(6): 1167-81, 2015.
Article in English | MEDLINE | ID: mdl-24594433

ABSTRACT

Depletion of alloreactive T-lymphocytes from allogeneic bone marrow transplants 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.


Subject(s)
Immunotoxins/toxicity , Lymphocyte Depletion/methods , Ribosome Inactivating Proteins, Type 1/toxicity , T-Lymphocytes/immunology , Animals , Antibodies, Monoclonal/metabolism , CD4-Positive T-Lymphocytes/metabolism , Cell Membrane/drug effects , Cell Membrane/metabolism , Cytotoxicity, Immunologic/drug effects , Endocytosis/drug effects , Female , Forkhead Transcription Factors/metabolism , Graft vs Host Disease/immunology , Graft vs Host Disease/prevention & control , Hematopoietic Stem Cell Transplantation , Humans , Leukemia/immunology , Leukemia/pathology , Lymphocyte Activation/drug effects , Lymphocyte Culture Test, Mixed , Mice , Protein Binding/drug effects , Saporins , T-Lymphocytes/drug effects , Transplantation, Homologous , Tumor Necrosis Factor Receptor Superfamily, Member 9/metabolism
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