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FAILURE OF A CD18/ANTI-LFAl MONOCLONAL ANTIBODY PATIENTS RECEIVING T-DEPLETED ALLOGENEIC BONE INFUSION TO PREVENT GRAFT REJECTION IN LEUKEMIC MARROW TRANSPLANTATION
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1989
Year
Cell TherapyImmunologyCommon Beta ChainImmunotherapyEarly SepsisOrthopaedic SurgeryBone Marrow FailureHematologyRadiation OncologyCell TransplantationHealth SciencesTransplantationMarrow TransplantationAutoimmune DiseaseAutoimmunityBlood TransplantationTransplant RejectionCd18 AntibodiesImmunosuppressive TherapyMedicineGraft Rejection
CD18 antibodies react with the common beta chain of the human leukocyte function antigen (LFA1)* and thus block the functions mediated by the three identified molecules in humans. A murine CD18 monoclonal antibody was infused in 8 leukemic patients receiving allogeneic T-depleted bone marrow transplantation in order to prevent graft rejection. This was part of the conditioning, including total-body irradiation and high-dose chemotherapy, given to all patients. To prevent graft-versus-host disease the donor bone marrow T cells were depleted using complement-mediated cytolysis or a ricin A conjugate immunotoxin, and cyclosporine or methotrexate were given posttransplant. A persistent level of free circulating anti-LFA1 antibody was detected in 5/8 patients. Despite this, 5 graft failures occurred, with 2 patients experiencing late rejection (days 60 and 97) following HLA-identical transplantation and 3 patients having no engraftment following haplo-mismatched transplant. One other patient died of early sepsis. Only 2 patients (who differed at 1 HLA locus from their donor) are alive with long-term complete chimerism (300 and 315 days). Transient inhibition of recipients' leukocyte functions with an anti-LFA1 antibody did not appear to facilitate engraftment of allogeneic T-depleted marrow transplantation for leukemias.