Abstract:In order to evaluate the possible reactivation of human herpesviruses 6 (HHV-6) and 7 (HHV-7) after heart transplantation, buffy-coat and plasma specimens from 21 transplant patients and 56 healthy blood donors were examined for HHV-6 and HHV-7 DNA by polymerase chain reaction. Human herpesvirus 6 and HHV-7 infection or reactivation has been suggested to play a role in cytomegalovirus disease progression in renal transplant recipients. In the present study, however, no significant difference in the prevalence … Show more
“…The controversy about the influence between HHV‐6 and HHV‐7 replication and CMV infection is not resolved [8, 9]. In this study, we could observed that CMV replication was longer in the presence of HHV‐6 viremia: 40 ± 25 days versus 18 ± 16 days ( P = 0.0001).…”
Section: Incidence Apparition and Duration Of CMV Hhv‐6 And Hhv‐7 Vmentioning
“…The controversy about the influence between HHV‐6 and HHV‐7 replication and CMV infection is not resolved [8, 9]. In this study, we could observed that CMV replication was longer in the presence of HHV‐6 viremia: 40 ± 25 days versus 18 ± 16 days ( P = 0.0001).…”
Section: Incidence Apparition and Duration Of CMV Hhv‐6 And Hhv‐7 Vmentioning
“…It is also important to screen adult recipients for antibodies to EBV, since seronegative recipients of organs from infected donors are at increased risk for the development of post-transplant lymphoproliferative disorder [42]. Screening of donor or recipient for human herpesvirus-6 (HHV-6) or HHV-8 is not routinely performed; the impact of HHV-6 infection in heart transplant patients has not yet been clearly defined [43], and the rare occurrence of Kaposi's sarcoma among heart transplant recipients (less than 1%) [44] makes population screening impractical.…”
Section: Donor and Recipient Serologic Screeningmentioning
Screening of recipients and donors of cardiac allografts for infectious pathogens, and the use of appropriate immunization and antimicrobial prophylaxis strategies, remain important for the control of infection following heart transplantation. However, the risk of infectious complications in a particular patient must often be weighed against the risk of delaying or denying allograft transplantation. In addition, the ongoing degree of immunosuppression and its contribution to the risk for infectious complications should also be considered to guide the length of prophylactic antimicrobial therapy and provide optimal patient care.
“…The development of a sensitive and rapid diagnostic assay is necessary for the early initiation of antiviral therapy to avoid complications and loss of the transplanted organ [1,2,5]. A prospective laboratory and clinical study that involved a subgroup of kidney transplant recipients was performed to assess a longitudinal analysis of the clinical impact of plasma herpesvirus viremia and CMV urine excretion in this population.…”
Section: Longitudinal Study Of Herpesviruses In Kidney Transplant Recmentioning
We compared a multiplex polymerase chain reaction assay and a shell vial assay for the detection of herpesviruses infection in 13 Cuban patients who had received kidney transplants. Cytomegalovirus and human herpesvirus 6 were detected in these patients.
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