Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant

A. P. Mitterhofer, V. Pietropaolo, M. Barile, F. Tinti, D. Fioriti, M. Mischitelli, A. Limonta, A. Meçule, G. Ferretti, L. Poli, F. Chiarini, P. B. Berloco, G. Taliani

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Abstract

Polyomavirus BK (BKV) infection is ubiquitous in the human population. Under immunosuppression, BKV can undergo reactivation resulting in viral replication. What really happens in the early hours posttransplantation is not clearly defined; the meaning of early viremia and viruria is not clear. BKV viremia is considered a marker of infection. The aim of our study was to investigate the prevalence of early BKV infection in kidney transplant patients, to evaluate the relationship to infections at 3 and 6 months and the association with recipient, donor, and graft features. We enrolled 36 kidney transplanted patients from May 2006 to April 2007. BKV load was measured on plasma and urine samples by Q-PCR at 12 hours (T0/early) as well as 3 (T3) and 6 (T6) months thereafter. A high percentage of BKV infections were detectable in the first hours after transplantation (33.3%), which remained unchanged to month 6 post transplantation. Moreover, patients who were positive at T0 had a high probability of remaining positive thereafter. The number of copies in plasma samples tended to increase at 3 months and to decrease thereafter, whereas the urine viral load tended to steadily increase. Among BKV-positive patients, we identified 2 groups according to viremic state at T0: 9 patients (group A); who were already positive and remained so to T6 5 and 3 patients who turned positive at 3 or at 6 months, respectively (group B). Group A included 75% of positive patients at T0 and 90% of positive patients at either T3 or T6 (P = .007). The most important contribution of our study was to highlight the presence of BKV infection in renal transplant recipients from the first hours posttransplantation. This condition seemed to be the most important risk factor for persistent infection in the first 6 months.

Original languageEnglish
Pages (from-to)1142-1145
Number of pages4
JournalTransplantation Proceedings
Volume42
Issue number4
DOIs
Publication statusPublished - May 2010

Fingerprint

BK Virus
Transplants
Kidney
Infection
Viremia
Transplantation
Urine
Viral Load
Immunosuppression
Tissue Donors
Polymerase Chain Reaction

ASJC Scopus subject areas

  • Surgery
  • Transplantation

Cite this

Mitterhofer, A. P., Pietropaolo, V., Barile, M., Tinti, F., Fioriti, D., Mischitelli, M., ... Taliani, G. (2010). Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant. Transplantation Proceedings, 42(4), 1142-1145. https://doi.org/10.1016/j.transproceed.2010.03.130

Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant. / Mitterhofer, A. P.; Pietropaolo, V.; Barile, M.; Tinti, F.; Fioriti, D.; Mischitelli, M.; Limonta, A.; Meçule, A.; Ferretti, G.; Poli, L.; Chiarini, F.; Berloco, P. B.; Taliani, G.

In: Transplantation Proceedings, Vol. 42, No. 4, 05.2010, p. 1142-1145.

Research output: Contribution to journalArticle

Mitterhofer, AP, Pietropaolo, V, Barile, M, Tinti, F, Fioriti, D, Mischitelli, M, Limonta, A, Meçule, A, Ferretti, G, Poli, L, Chiarini, F, Berloco, PB & Taliani, G 2010, 'Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant', Transplantation Proceedings, vol. 42, no. 4, pp. 1142-1145. https://doi.org/10.1016/j.transproceed.2010.03.130
Mitterhofer AP, Pietropaolo V, Barile M, Tinti F, Fioriti D, Mischitelli M et al. Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant. Transplantation Proceedings. 2010 May;42(4):1142-1145. https://doi.org/10.1016/j.transproceed.2010.03.130
Mitterhofer, A. P. ; Pietropaolo, V. ; Barile, M. ; Tinti, F. ; Fioriti, D. ; Mischitelli, M. ; Limonta, A. ; Meçule, A. ; Ferretti, G. ; Poli, L. ; Chiarini, F. ; Berloco, P. B. ; Taliani, G. / Meaning of Early Polyomavirus-BK Replication Post Kidney Transplant. In: Transplantation Proceedings. 2010 ; Vol. 42, No. 4. pp. 1142-1145.
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abstract = "Polyomavirus BK (BKV) infection is ubiquitous in the human population. Under immunosuppression, BKV can undergo reactivation resulting in viral replication. What really happens in the early hours posttransplantation is not clearly defined; the meaning of early viremia and viruria is not clear. BKV viremia is considered a marker of infection. The aim of our study was to investigate the prevalence of early BKV infection in kidney transplant patients, to evaluate the relationship to infections at 3 and 6 months and the association with recipient, donor, and graft features. We enrolled 36 kidney transplanted patients from May 2006 to April 2007. BKV load was measured on plasma and urine samples by Q-PCR at 12 hours (T0/early) as well as 3 (T3) and 6 (T6) months thereafter. A high percentage of BKV infections were detectable in the first hours after transplantation (33.3{\%}), which remained unchanged to month 6 post transplantation. Moreover, patients who were positive at T0 had a high probability of remaining positive thereafter. The number of copies in plasma samples tended to increase at 3 months and to decrease thereafter, whereas the urine viral load tended to steadily increase. Among BKV-positive patients, we identified 2 groups according to viremic state at T0: 9 patients (group A); who were already positive and remained so to T6 5 and 3 patients who turned positive at 3 or at 6 months, respectively (group B). Group A included 75{\%} of positive patients at T0 and 90{\%} of positive patients at either T3 or T6 (P = .007). The most important contribution of our study was to highlight the presence of BKV infection in renal transplant recipients from the first hours posttransplantation. This condition seemed to be the most important risk factor for persistent infection in the first 6 months.",
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