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Prepublished online as a Blood First Edition Paper on July 5, 2002; DOI 10.1182/blood-2002-04-1197.
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Blood, 15 November 2002, Vol. 100, No. 10, pp. 3825-3827
BRIEF REPORT
Evaluation of KIR ligand incompatibility in mismatched unrelated
donor hematopoietic transplants
Stella M. Davies,
Loredana Ruggieri,
Todd DeFor,
John E. Wagner,
Daniel J. Weisdorf,
Jeffrey S. Miller,
Andrea Velardi, and
Bruce R. Blazar
From the Blood and Marrow Transplant Program,
University of Minnesota, Minneapolis; and Department of Clinical and
Experimental Medicine, Division of Hematology and Clinical Immunology,
Perugia University School of Medicine, Perugia, Italy.
One of the functions of HLA class I alleles is interaction with
natural killer (NK) cells. Receptors termed killer immunoglobulinlike receptors (KIRs) on NK cells recognize groups of HLA class I alleles, and interaction between receptor and class I allele inhibits reactivity of the NK cell. Failure to recognize the appropriate KIR ligand on a
mismatched cell can trigger NK cell elimination of that target cell.
Recent analysis of haploidentical hematopoietic transplantations has
shown a reduction of graft failure, graft-versus-host disease, and
relapse in those with KIR ligand incompatibility in the
graft-versus-host direction. In this study we analyzed the
effect of KIR ligand incompatibility on outcomes of unrelated donor
bone marrow transplantations. The data show no advantage for
KIR ligand incompatibility in this clinical setting as assessed by
HLA-Bw4 and HLA-C alleles. It is possible that there will be a benefit
of NK cell alloreactivity if strategies of haploidentical
transplantation are used: high stem cell doses, extensive T-cell
depletion, and no postgrafting immune suppression.

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