Author/Authors :
Folkmane، Inese Folkmane نويسنده Latvian Transplantation Centre, Pauls Stradi?? University Hospital, Pilso?u iela 13, Rîga, LV-1002, LATVIA; , , Eapenko، Svetlana نويسنده Augusts Kirhen?teins Institute of Microbiology and Virology, Rîga Stradi?? University, Râtsupîtes iela 5, Rîga, LV-1067, LATVIA , , Adamsone، Inara نويسنده Latvian Transplantation Centre, Pauls Stradi?? University Hospital, Pilso?u iela 13, Rîga, LV-1002, LATVIA; , , Folkmane، Elizabete نويسنده Faculty of Medicine, University of Latvia, ?arlotes iela 1a, Rîga, LV-1001, LATVIA , , Murovska، Modra نويسنده Faculty of Medicine, University of Latvia, ?arlotes iela 1a, Rîga, LV-1001, LATVIA ,
Abstract :
Human herpesviruses HHV-6 and HHV-7 reactivation in transplantation is associated with indirect
immunomodulatory effects, such as cytomegalovirus (CMV) disease, increased opportunistic infections,
graft dysfunction and acute rejection (AR). In this study, we analysed the clinical and immunological
outcomes in renal transplant recipients (RTR) with active HHV-6 and HHV-7
infection. Between January 2007 and December 2007, clinical, virological and immunological
tests were carried out in 46 RTR. The patients were divided into three groups: with active HHV-6
infection; with active HHV-7 infection; and without infection (control). The mean follow-up was
14 ± 2.5 months. At three months after renal transplantation (RT), active CMV infection was present
in 12 (26%); HHV-6 in four (8.6%); and HHV-7 in nine (19.5%) of RTR. Active B-herpesviruses
infection was not associated with more frequent AR and worsening of graft function in
recipients at different times after RT. The lymphocyte subsets (CD3+; CD4+ and CD8+ cell count)
were considerably lower in RTR before RT. At 3 months after RT CD19+ and CD25+ cell counts
were significantly increased in the HHV-7 group compared with the control group (P < 0.05). Significant
differences were not found in clinical and immunological outcomes between patients with
active B-herpesviruses infection and those without active B-herpesviruses infection.