%0 Journal Article
%T A paradigm linking herpesvirus immediate-early gene expression apoptosis and myalgic encephalomyelitis chronic fatigue syndrome
%A A Martin Lerner
%A Safedin Beqaj
%J Virus Adaptation and Treatment
%D 2011
%I Dove Medical Press
%R http://dx.doi.org/10.2147/VAAT.S15105
%X paradigm linking herpesvirus immediate-early gene expression apoptosis and myalgic encephalomyelitis chronic fatigue syndrome Original Research (4320) Total Article Views Authors: A Martin Lerner, Safedin Beqaj Published Date February 2011 Volume 2011:3 Pages 19 - 24 DOI: http://dx.doi.org/10.2147/VAAT.S15105 A Martin Lerner1, Safedin Beqaj2 1Department of Medicine, William Beaumont Hospital, Royal Oak, MI, USA; 2DCL Medical Laboratories, Indianapolis, IN, USA Abstract: There is no accepted science to relate herpesviruses (Epstein¨CBarr virus [EBV], human cytomegalovirus [HCMV], and human herpesvirus 6 [HHV6]) as causes of myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS). ME/CFS patients have elevated serum immunoglobulin (Ig)G serum antibody titers to EBV, HCMV, and HHV6, but there is no herpesvirus DNA-emia, herpesvirus antigenemia, or uniformly elevated IgM serum antibody titers to the complete virions. We propose that herpesvirus EBV, HCMV, and HHV6 immediate-early gene expression in ME/CFS patients leads to host cell dysregulation and host cell apoptosis without lytic herpesvirus replication. Specific antiviral nucleosides, which alleviate ME/CFS, namely valacyclovir for EBV ME/CFS and valganciclovir for HCMV/HHV6 ME/CFS, inhibit herpesvirus DNA polymerases and/or thymidine kinase functions, thus inhibiting lytic virus replication. New host cell recruitment thus ceases. In the absence of new herpesvirus, nonpermissive herpesvirus replication stops, and ME/CFS recovery ensues.
%K ME/CFS
%K Epstein¨CBarr virus (EBV)
%K human cytomegalovirus (HCMV)
%K HHV6
%K abortive replication
%U https://www.dovepress.com/a-paradigm-linking-herpesvirus-immediate-early-gene-expression-apoptos-peer-reviewed-article-VAAT