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Detection of Epstein Barr Virus in Renal Transplant Recipients: Two Centers Study
حيدر صباح كاظم
Authors : Sahar A. Shams-aldein, Ahmed S. Abdlameer, Asmaa B. Al-Obaidi, Haider S. Kadhim, Ali J.Al-Saedi
Background: Viruses are among the most common causes of opportunistic infections after transplantation. The risk for viral infection is a function of the specific virus encountered and the intensity of immune suppression used to prevent graft rejection.Epstein-Barr virus infection has also been implicated as co-factor in acute and chronic rejection syndromes. Objective: Detection of Epstein-Barr viremia in renal transplant recipients. Methods: Fifty seven (57) renal transplant recipients were enrolled in this study. Plasma samples were taken from all renal transplant subjects. Screening of Epstein-Barr virus was first done by serology viamono spot test, then, viral DNA of Epstein-Barr viruswas extracted from 200 µl plasma samples and Epstein-Barr virus DNA was detected and measured by Taqman quantitative real-time PCR. Results 19/57 (33 %) of renal transplant subjects had Epstein-Barr virus viremia and the viral load ranged from 7100 to 16.165 copies/ml. Serology of all RT subjects showed negative heterophil antibody except for one patient had positive hetrophil antibody. Conclusion The current study showed that Epstein-Barr virus might be considered as an important cause of renal impairment and allograft loss in renaltransplant subjects. And Epstein-Barr virus seems associated with post transplantation renal impairment and/or kidney rejection. Real-time PCR is a very sensitive and specific method for the detection of Epstein-Barr viremia in renal transplant subjects. Key words Epstein-Barr virus, Renal transplantation, real-time PCR

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July 2015