• Biol. Blood Marrow Transplant. · Aug 2006

    Multicenter Study Clinical Trial

    KIR ligands and prediction of relapse after unrelated donor hematopoietic cell transplantation for hematologic malignancy.

    • Katharine C Hsu, Ted Gooley, Mari Malkki, Clara Pinto-Agnello, Bo Dupont, Jean-Denis Bignon, Martin Bornhäuser, Frank Christiansen, Alois Gratwohl, Yasuo Morishima, Machteld Oudshoorn, Olle Ringden, Jon J van Rood, Effie Petersdorf, and International Histocompatibility Working Group.
    • Adult Allogeneic Bone Marrow Transplantation Service, Memorial Hospital, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA. hsuk@mskcc.org
    • Biol. Blood Marrow Transplant. 2006 Aug 1; 12 (8): 828-36.

    AbstractRecurrent malignancy remains a significant complication after allogeneic hematopoietic cell transplantation (HCT). Efforts to decrease relapse have included donor lymphocyte infusion to stimulate donor anti-recipient T-cell allorecognition of major and minor histocompatibility differences. Recently, alloreactive effects of donor natural killer cell-mediated inhibitory killer immunoglobulin-like receptor (KIR) recognition of recipient HLA-C and -B ligands have been described. We examined KIR ligand effects on risk of relapse in 1770 patients undergoing myeloablative T-replete HCT from HLA-matched or -mismatched unrelated donors for the treatment of myeloid and lymphoid leukemias. KIR ligands defined by HLA-B and -C genotypes were used to determine donor-recipient ligand incompatibility or recipient lack of KIR ligand. Among HLA-mismatched transplantations, recipient homozygosity for HLA-B or -C KIR epitopes predicted lack of KIR ligand and was associated with a decreased hazard of relapse (hazard ratio, 0.61; 95% confidence interval, .043-0.85; P = .004). Absence of HLA-C group 2 or HLA-Bw4 KIR ligands was associated with lower hazards of relapse (hazard ratio, 0.47; 95% confidence interval, 0.28-0.79, P = .004; hazard ratio, 0.56; 95% confidence interval, 0.33-0.97; P = .04, respectively). The decrease in hazard of relapse in patients with acute myelogenous leukemia was similar to that in patients with chronic myelogenous leukemia and acute lymphoblastic leukemia (P = .95). Recipient homozygosity for HLA-B or -C epitopes that define KIR ligands is likely to be a predictive factor for leukemia relapse after myeloablative HCT from HLA-mismatched unrelated donors. This effect was not observed in HLA-identical unrelated transplants.

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