1. Detection of viral DNA in kidney graft preservation and washing solutions is predictive of posttransplant infections in pediatric recipients
- Author
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Alejandro Espadas De Arias, Giorgio Palù, Luisa Murer, Piergiorgio Gamba, Giulia Ghirardo, Luisa Barzon, Manuela Della Vella, Maria Angela Biasolo, Monia Pacenti, and Giovanni Franco Zanon
- Subjects
Human cytomegalovirus ,Adult ,Male ,Herpesvirus 4, Human ,Adolescent ,viruses ,Urinary system ,Organ Preservation Solutions ,Cytomegalovirus ,Kaplan-Meier Estimate ,Virus ,Serology ,Young Adult ,Predictive Value of Tests ,hemic and lymphatic diseases ,Biopsy ,medicine ,Parvovirus B19, Human ,Immunology and Allergy ,Humans ,Serologic Tests ,Risk factor ,Child ,Retrospective Studies ,medicine.diagnostic_test ,biology ,Parvovirus ,virus diseases ,Infant ,medicine.disease ,biology.organism_classification ,Kidney Transplantation ,DNA Virus Infections ,Transplantation ,surgical procedures, operative ,Infectious Diseases ,BK Virus ,Child, Preschool ,Immunology ,DNA, Viral ,Female - Abstract
BACKGROUND In pediatric kidney transplant recipients, viral infections occur soon after transplant and may be transmitted from the graft. METHODS This study of 75 pediatric kidney transplants investigated whether genome sequences of parvovirus B19, Epstein-Barr virus (EBV), human cytomegalovirus (HCMV), and BK polyomavirus (BKV) could be detected in kidney graft samples (graft biopsy samples and preservation and washing solutions) collected before implantation and whether their presence was a risk factor for infections in the recipient. RESULTS B19 DNA was detected in approximately 30% of graft biopsy samples, preservation solutions, and washing solutions; EBV DNA was detected in approximately 20% of preservation and washing solutions but rarely in biopsy samples; and HCMV DNA and BKV DNA were rarely detected in graft biopsy samples. Seronegative recipients of B19 DNA-positive and EBV DNA-positive grafts had a significantly higher risk of infection during the early posttransplant period than did recipients of negative grafts. In particular, none of the B19-seronegative recipients of B19 DNA-negative grafts experienced infection soon after transplant, whereas most recipients of B19 DNA-positive grafts experienced infection within the first month after transplant. CONCLUSIONS Molecular testing of donor grafts for viruses that infect circulating and resident cells in the graft-such as B19 in the kidney-could be useful (in association with donor/recipient serostatus) for identifying recipients at high risk for posttransplant infections.
- Published
- 2009