T-CELL AND NK CELL-MEDIATED GRAFT-VERSUS-LEUKEMIA REACTIVITY FOLLOWING DONOR BUFFY COAT TRANSFUSION TO TREAT RELAPSE AFTER MARROW TRANSPLANTATION FOR CHRONIC MYELOID-LEUKEMIA
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JIANG, YZ
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLAND
JIANG, YZ
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CULLIS, JO
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLAND
CULLIS, JO
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KANFER, EJ
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLAND
KANFER, EJ
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GOLDMAN, JM
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLAND
GOLDMAN, JM
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BARRETT, AJ
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT HAEMATOL,DU CANE RD,LONDON W12 0NN,ENGLAND
Two patients with chronic myeloid leukaemia in cytogenetic relapse following T lymphocyte-depleted BMT were treated with transfusions of donor buffy coat leucocytes. In both patients the marrow reverted to a completely normal karyotype and was negative for the BCR-ABL fusion gene transcript by polymerase chain reaction analysis. Before buffy coat transfusion the cytotoxic T lymphocyte precursor frequency against pre-BMT patient leukaemia cells (Lk-CTLP) was lower than that against pre-BMT patient PHA-transformed lymphocytes (Ly-CTLP) in both cases. At 2 weeks (case 1) and 8 weeks (case 2) after transfusion this ratio inverted so that Lk-CTLP predominated. Natural killer (NK) function fell initially and then recovered to exceed pre-transfusion values prior to normalization of the bone marrow karyotype. These changes in cytotoxic T lymphocytes and NK cells following donor buffy coat transfusions for patients with relapsed chronic myeloid leukaemia after marrow transplantation support the concept of a graft-versus-leukaemia effect mediated by both MHC restricted and non-restricted pathways.