Cytomegalovirus infection after bone marrow transplantation: an association with acute graft-v-host disease

W Miller, P Flynn, J McCullough, HHJ Balfour… - 1986 - ashpublications.org
W Miller, P Flynn, J McCullough, HHJ Balfour, A Goldman, R Haake, P McGlave, N Ramsay…
1986ashpublications.org
Among 181 patients undergoing allogeneic bone marrow transplantation over a five-year
period (1978 through 1982), cytomegalovirus (CMV) infection was a frequent and often
lethal complication. Recipient pretransplant serology was the most important predictor of
posttransplant CMV infection. CMV infection occurred in 26/137 seronegative recipients and
in 28/44 seropositive recipients (P less than. 001). Among patients who developed CMV
infection, the time to infection was identical in seronegative and seropositive patients …
Abstract
Among 181 patients undergoing allogeneic bone marrow transplantation over a five-year period (1978 through 1982), cytomegalovirus (CMV) infection was a frequent and often lethal complication. Recipient pretransplant serology was the most important predictor of posttransplant CMV infection. CMV infection occurred in 26/137 seronegative recipients and in 28/44 seropositive recipients (P less than .001). Among patients who developed CMV infection, the time to infection was identical in seronegative and seropositive patients (median, 71 days post transplant). Bone marrow donor CMV serology did not significantly influence CMV infection rate. CMV infection was strongly associated with acute graft-v-host disease (AGVHD), occurring in 34/81 patients with AGVHD and 20/100 without GVHD (P less than .001). AGVHD preceded CMV infection by 33.7 days (mean) in patients developing both complications. Patients who developed CMV infections had also received more cellular blood products post transplant. These data suggest that CMV infection may occur through reactivation of latent virus (in seropositive recipients) or through exogenous exposure, possibly through transfused blood products, but that duration of immunoincompetence may be more critical than route of exposure in timing of clinically evident CMV infection. Prophylaxis tailored to the likely infectious source and more effective GVHD prevention both may be critical in preventing CMV infection after bone marrow transplantation.
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