## Abstract Human herpesvirus 7 (HHV‐7) is the least studied β‐herpesvirus in transplant settings. This prospective study examined the activity of HHV‐7 during the first 12 weeks post‐stem cell transplant in 59 paediatric patients. The presence of HHV‐7, human cytomegalovirus (HCMV) and human herpe
Confirmation of the low clinical effect of human herpesvirus-6 and -7 infections after renal transplantation
✍ Scribed by Delphine Caïola; Alexandre Karras; Philippe Flandre; David Boutolleau; Catherine Scieux; Henri Agut; Christophe Legendre; Agnès Gautheret-Dejean
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 153 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
Human herpesvirus‐6 and ‐7 (HHV‐6 and HHV‐7) may lead to pathological manifestations in renal transplant recipients. The aim of this study was to investigate beta‐herpesvirus infections in 50 adult kidney transplant recipients after transplantation to examine the effect, interactions, and pathogenic consequences of infection and the effect of immunosuppressive regimens and Human cytomegalovirus (HCMV) prophylaxis with VACV. Beta‐herpesviruses loads in the blood of 50 adult kidney transplant recipients over a 6‐month period after transplantation and 198 blood donors were determined using polymerase chain reaction. The rate of HHV‐6 detection in peripheral mononuclear cells (PBMCs) was higher in patients with end‐stage renal disease and during the post‐transplantation follow‐up than in healthy subjects (33% and 68% vs. 12%, respectively). The detection rate of HHV‐7 in PBMCs was similar between patients, both before grafting and during the follow‐up for transplant recipients (69% and 88%, respectively), and healthy subjects (78%), and correlated with the number of lymphocytes. HCMV in plasma was detected only in patients during the post‐transplant period (24%). VACV prophylaxis had no negative effect on the replication of HHV‐6 or HHV‐7, and univariate analyses demonstrated associations between HHV‐6 infection and acute graft rejection [Odds ratio (OR) = 2.94, 95% confidence interval (CI), 1.05–8.2, __P =__0.04], and between HHV‐7 infection and cholestasis [OR = 2.61 (95% CI, 1.08–6.3), __P =__0.03]. Immunosuppressive regimens had no effect on beta‐herpesviruses infections. This study revealed the differing behavior of HCMV, HHV‐6, and HHV‐7 in kidney transplant recipients, and confirmed the association of HHV‐6 with graft rejection. J. Med. Virol. 84:450–456, 2012. © 2011 Wiley Periodicals, Inc.
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Because cytomegalovirus (CMV) is an important opportunistic infection after liver transplant, we conducted a prospective study to see if the same applied to human herpesviruses (HHV)-6 and -7. We used polymerase chain reaction (PCR) methods optimised to detect active, not latent, infection and studi
## Abstract Sera from 50 orthotopic liver transplant recipients were examined for antibodies to human herpesvirus 6 (HHV‐6) and Cytomegalovirus (CMV), and the findings correlated with the clinical condition of the patients. Both primary and secondary HHV‐6 infections were detected sero‐logically fo
Diagnosis of significant infections by human herpesvirus 6 (HHV6) and 7 (HHV7) in transplant patients has proved difficult because both viruses are ubiquitous and can cause persistent infections in their hosts. The significance of viral DNA detected in peripheral blood leukocytes (PBLs; DNAemia) by