TY - JOUR
T1 - Acquisition of Donor Strains of Cytomegalovirus by Renal-Transplant Recipients
AU - Chou, Sunwen
PY - 1986/5/29
Y1 - 1986/5/29
N2 - To determine the source of post-transplantation cytomegalovirus (CMV) infection in renal-transplant recipients, viral isolates were collected from pairs of patients who received kidneys from the same cadaver. Among 36 pairs of recipients, CMV viruria or viremia occurred in both members of 4 pairs and in one member of 11 pairs. Restriction-enzyme analysis of viral DNA revealed 15 distinct strains of CMV among viral isolates from these 19 patients. In all four pairs in which both members shed CMV, both recipients shed the same strain, suggesting that the virus was of donor origin. In three of these pairs, one member had been seropositive for CMV before transplantation. One seropositive recipient was simultaneously shedding two strains of CMV after transplantation; one strain was of donor origin. Two patients who had CMV viruria before receiving grafts from a seropositive donor shed a different CMV strain two months after grafting. These findings indicate that cadaveric grafts can transmit an identifiable strain of CMV to recipients, and that seropositive recipients can be reinfected by a new CMV strain from the donor after transplantation. (N Engl J Med 1986;314:1418–23.), ORGAN transplantation is frequently complicated by cytomegalovirus (CMV) infection, which may be clinically inapparent or may cause problems ranging from fever to pneumonia or retinitis. Abundant epidemiologic data indicate that CMV infection can be transmitted from donors of transplant organs to their recipients, even though a donor has no evidence of CMV disease and culture of the donated organ reveals no infectious CMV.1 Specifically, when an organ from a CMV-seropositive donor is transplanted into a seronegative recipient, that recipient has a high risk of acquiring CMV infection after transplantation, whereas an organ from a CMV-seronegative donor carries little or no…
AB - To determine the source of post-transplantation cytomegalovirus (CMV) infection in renal-transplant recipients, viral isolates were collected from pairs of patients who received kidneys from the same cadaver. Among 36 pairs of recipients, CMV viruria or viremia occurred in both members of 4 pairs and in one member of 11 pairs. Restriction-enzyme analysis of viral DNA revealed 15 distinct strains of CMV among viral isolates from these 19 patients. In all four pairs in which both members shed CMV, both recipients shed the same strain, suggesting that the virus was of donor origin. In three of these pairs, one member had been seropositive for CMV before transplantation. One seropositive recipient was simultaneously shedding two strains of CMV after transplantation; one strain was of donor origin. Two patients who had CMV viruria before receiving grafts from a seropositive donor shed a different CMV strain two months after grafting. These findings indicate that cadaveric grafts can transmit an identifiable strain of CMV to recipients, and that seropositive recipients can be reinfected by a new CMV strain from the donor after transplantation. (N Engl J Med 1986;314:1418–23.), ORGAN transplantation is frequently complicated by cytomegalovirus (CMV) infection, which may be clinically inapparent or may cause problems ranging from fever to pneumonia or retinitis. Abundant epidemiologic data indicate that CMV infection can be transmitted from donors of transplant organs to their recipients, even though a donor has no evidence of CMV disease and culture of the donated organ reveals no infectious CMV.1 Specifically, when an organ from a CMV-seropositive donor is transplanted into a seronegative recipient, that recipient has a high risk of acquiring CMV infection after transplantation, whereas an organ from a CMV-seronegative donor carries little or no…
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U2 - 10.1056/NEJM198605293142205
DO - 10.1056/NEJM198605293142205
M3 - Article
C2 - 3010114
AN - SCOPUS:0022637288
SN - 0028-4793
VL - 314
SP - 1418
EP - 1423
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 22
ER -