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Blood, 1 February 2006, Vol. 107, No. 3, pp. 1230-1232.
Prepublished online as a Blood First Edition Paper on October 20, 2005; DOI 10.1182/blood-2005-03-1039.


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TRANSPLANTATION
Brief report

Donor KIR genotype has a major influence on the rate of cytomegalovirus reactivation following T-cell replete stem cell transplantation

Mark Cook, David Briggs, Charles Craddock, Premini Mahendra, Donald Milligan, Christopher Fegan, Philip Darbyshire, Sarah Lawson, Elizabeth Boxall, and Paul Moss

From the Department of Haematology, University Hospital Birmingham NHS Foundation Trust, Edgbaston, Birmingham, United Kingdom; Department of Histocompatibility and Immunogenetics, National Blood Service Birmingham, Edgbaston, Birmingham, United Kingdom; CRUK Institute for Cancer Studies, University of Birmingham, Birmingham, United Kingdom; Department of Haematology, Heart of England NHS Foundation Trust, Birmingham, United Kingdom; Department of Haematology, Birmingham Children's Hospital, Birmingham, United Kingdom; and West Midlands Public Health Laboratory, Health Protection Agency, Birmingham, United Kingdom.

Reactivation of cytomegalovirus (CMV) is a common complication following allogeneic stem cell transplantation. Genetic determinants in the host and donor that may influence the rate of reactivation are currently unknown. Viral replication is controlled by T cells and natural killer (NK) cells and these share expression of killer immunoglobulin-like receptors (KIRs). We analyzed whether activatory KIRs carried by the donor influenced the subsequent rate of CMV reactivation in the patient. In transplantations involving siblings where both donor and recipient were CMV seropositive, donors with more than one activating KIR gene were associated with a 65% reduction in CMV reactivation. Multivariate analysis confirmed a significantly reduced risk of CMV reactivation in sibling transplantations where the donor had more than one activating KIR. Reduced-intensity transplantation and graft-versus-host disease grade 2 or higher were associated with an increased risk of CMV reactivation. This observation indicates that activating KIRs play an important role in the cellular control of CMV reactivation.


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