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Activation of human herpesviruses 6 and 7 in patients with chronic fatigue syndrome.

Authors :
Chapenko S
Krumina A
Kozireva S
Nora Z
Sultanova A
Viksna L
Murovska M
Source :
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology [J Clin Virol] 2006 Dec; Vol. 37 Suppl 1, pp. S47-51.
Publication Year :
2006

Abstract

Background: Human herpesvirus 6 (HHV-6) and 7 (HHV-7) have been suggested as possible triggering agents for chronic fatigue syndrome (CFS).<br />Objectives: To determine the possible association of HHV-6 and HHV-7 infections with CFS.<br />Study Design: The prevalence of latent/persistent and active viral infections by nPCR, characteristic of HHV-6 variants using restriction endonuclease analysis and changes of lymphocyte subsets in peripheral blood by laser flow-cytometry in 17 CFS patients was examined. In addition, 12 patients with unexplained chronic fatigue and 20 blood donors (BD) were studied.<br />Results: No difference in prevalence of latent/persistent single viral infections between the patients and BD was found but dual infection rate was significantly higher in CFS patients. Active HHV-6 and dual (HHV-6 + HHV-7) infections were detected in CFS patients only and frequency of HHV-7 reactivation was also significantly higher in these patients. HHV-6 variant B was predominant in CFS patients (12/13). The changes of immunological parameters in CFS patients with active dual infection were characterized by significant decrease of CD3+ and CD4+ T cells, significant increase of CD95+ cells and decrease of CD4+/CD8+ ratio.<br />Conclusions: HHV-6 and HHV-7 may be involved in the pathogenesis of CFS and reactivation of both viruses may provoke changes in the phenotype of circulating lymphocytes.

Details

Language :
English
ISSN :
1386-6532
Volume :
37 Suppl 1
Database :
MEDLINE
Journal :
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
Publication Type :
Academic Journal
Accession number :
17276369
Full Text :
https://doi.org/10.1016/S1386-6532(06)70011-7